Small Molecules Modulator of Epigenetic Regulation and Their Therapeutic Applications

ABSTRACT

Disclosed are methods and compositions for modulating the function of transcription factors, especially transcription factors that recruit epigenetic regulators (histone modifying enzymes) to specific DNA promoters. The targeted transcription factors include but are not limited to the myocyte enhancing factor (MEF2), the forkhead/winged helix transcription factor FOXP3 and the transcription factor GATA3. Also disclosed are small molecule modulators of MEF2 and its associated factors that include but not limited to histone deacetylases (HDACs), p300/CBP and Cabin1 and the therapeutic applications thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/111,689, filed on Nov. 5, 2008, and Provisional Application No. 61/246,934, filed on Sep. 29, 2009. The above provisional applications are hereby incorporated herein by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT

This invention was made with support in part by the following grants from NIH R21AI49905, RO1HL076334, and RC1DA028790. Therefore, the U.S. government has certain rights.

FIELD OF THE INVENTION

The invention relates generally to the field of molecular medicine. In particular, the invention pertains to methods and compositions for modulating the function of transcription factors, especially transcription factors that recruit epigenetic regulators (histone modifying enzymes) to specific DNA promoters. The targeted transcription factors include but are not limited to the myocyte enhancing factor (MEF2), the forkhead/winged helix transcription factor FOXP3 and the transcription factor GATA3. More particularly, the invention pertains to small molecule modulators of MEF2 and its associated factors that include but not limited to histone deacetylases (HDACs), p300/CBP and Cabin1 and the therapeutic applications thereof.

BACKGROUND OF THE INVENTION

This invention relates to the use of small molecules for modulating the functions of transcription factors that are associated with certain diseases. Transcription factors are proteins that bind to specific DNA sequences and regulate gene expression either directly or through associated proteins such as co-activators and co-repressors, or by recruiting histone modifying enzymes such as histone acetyltransferases (HATs) and histone deacetylases (HDACs). Transcription factors play key roles in many biological processes by ensuring the appropriate level of gene expression. They can also be associated with certain disease states, if their ability to regulate transcription is aberrantly modified. The identification and development of small molecules that can selectively modulate the function of certain transcription factors, therefore, can lead to potentially new therapeutic applications. This invention is based on two basic ideas. One is to develop small molecules that bind a specific transcription factors such as MEF2, FOXP3 and GATA3 and modulate its interaction with transcription co-activators and co-repressors. The other is to develop small molecules to block the recruitment of HAT (such as p300 and CBP) and HDACs and other histone modifying enzymes (such as histone methyltransferases, and demethylases, DNA methyltransferases) and chromatin remodeling machineries to specific regions of chromatin.

In particular, this invention relates to the myocyte enhancer factor-2 (MEF2) which plays critical roles in the development and adaptive responses of the muscle, immune and nervous systems (Flavell et al., 2006; Kim et al., 2008; Mao et al., 1999; McKinsey et al., 2002; Pan et al., 2004; Potthoff and Olson, 2007; Youn and Liu, 2000; Youn et al., 1999). MEF2 has been implicated as a key regulator of hypertrophic responses in heart muscle cells. Heart hypertrophy induced by pathological stimuli can lead to heart failure in many forms of cardiovascular diseases.

MEF2 generally defines a family of transcription factors with four members: MEF2A, MEF2B, MEF2C and MEF2D. The importance of their function has been demonstrated in detail through the use of murine and Drosophila genetics (Potthoff and Olson, 2007). MEF2, in skeletal muscles where it was initially identified, together with myogenic basic helix-loop-helix transcription factors such as MyoD, promotes and maintains myogenesis (Molkentin and Olson, 1996). MEF2A, one member of the MEF2 family, has recently been coined as the “heart attack gene” because a mutation in this protein is linked to coronary artery disease (CAD) and myocardial infarction (MI) (Wang et al., 2003). These findings underlie a critical role of MEF2 in human heart diseases (Kim et al., 2008; Wei et al., 2008; Zhang et al., 2002).

MEF2 is now known to be a general transcriptional factor in many other cell types. For instance, MEF2 is one of the important transcriptional factors for mediating calcium signaling in lymph system development} (Pan et al., 2004; Youn and Liu, 2000; Youn et al., 1999). MEF2 regulates cytokine expression and immune responses. MEF2 also regulates transcription programs underlying neuronal survival and synaptic remodeling (Chen and Cepko, 2009; Flavell et al., 2006; Flavell and Greenberg, 2008; Flavell et al., 2008; Mao et al., 1999; Morrow et al., 2008; Shalizi et al., 2006; Shalizi and Bonni, 2005; Yang et al., 2009). These observations suggest that small molecules that modulate MEF2 function could have therapeutic effect in cardiac hypertrophy and heart failure, autoimmune diseases and transplant rejection, neurodegenerative diseases and pathological impairment of learning and memory (Fischer et al., 2007; Stefanko et al., 2009).

Inside cells, the action of MEF2 includes three distinct steps: (i) transcriptional repression; (ii) calcium-dependent de-repression; and (iii) transcription activation. Transcriptional repression by MEF2 depends on its association with a variety of transcriptional co-repressors with intrinsic or associated histone deacetylase (HDAC) activity. In T cells, MEF2 bind Cabin1, which in turn associate with class I HDACs such as HDAC1, HADC2 and HDAC3 (Youn and Liu, 2000). In muscle cells, MEF2 binds directly to class II HDACs such as HDAC4, HDAC5, and HDAC9 and inhibits the expression of specific genes involved in the development and adaptive responses of muscle (Chan et al., 2003; Gregoire et al., 2006; Gregoire and Yang, 2005; McKinsey et al., 2001, 2002; Miska et al., 1999; Sparrow et al., 1999). Mice whose HDAC5 or HDAC9 has been knocked out showed increased sensitivity to hypertrophic stimuli, suggesting important roles of class II HDACs in heart hypertrophy (Potthoff and Olson, 2007). These and other data indicate that MEF2 and Class II histone deacetylases (HDACs), and particularly HDAC5 and HDAC9, are key mediators of hypertrophic signals in cardiomyocytes. Ample data have suggested that the MEF2/class II HDAC pathway is potential therapeutic target for heart hypertrophy.

In response to specific calcium signals, Cabin1 and HDACs are removed from MEF2 (Potthoff and Olson, 2007). MEF2 then recruits co-activators such as p300 and CBP to turn on distinct programs by association with a variety of transcriptional activators and co-activators (McKinsey et al., 2001; Sartorelli et al., 1997; Slepak et al., 2001; Wei et al., 2008). A small increase of p300 has been shown to be necessary and sufficient to induce MEF2-dependent cardiac hypertrophy. MEF2 has a highly conserved N-terminal region (residues 2-93), consisting of the well-characterized MADS-box and a MEF2-specific domain (Shore and Sharrocks, 1995). The MADS-box/MEF2 domain is remarkably rich in function, mediating DNA binding, dimerization, and protein-protein interactions with a myriad of MEF2 transcription partners (McKinsey et al., 2001, 2002), including Cabin1, Class IIa HDACs and p300/CBP. It has been shown that the MADS-box/MEF2 domain in MEF2 is necessary and sufficient to bind with a small motif conserved in class II HDACs and Cabin1. The CH3 domain of p300 and CBP is also shown to bind the MADS-box/MEF2 domain.

Despite the extensive knowledge about MEF2's involvement in various cellular processes available in the art, it has heretofore been impossible to capitalize on the knowledge due the lack of suitable molecular tools. In particular, how to modulate the activity of MEF2 by small molecules has been a long standing challenge. This is because MEF2 is a relatively small transcription factor without any apparent enzymatic activity; its main function is to bind specific DNA and recruit transcription co-regulators such as Cabin1, class II HDACs and p300/CBP to specific promoters. This mode of function is generally considered not druggable or at least very difficult to target by small molecules. Discovery or creation of such molecules will facilitate further advances in this field and can lead to new mechanism-based and structure-based therapeutic applications for MEF2-associated diseases, including inflammation, autoimmune diseases, neurodegenerative diseases, cancer, and cardiovascular disease.

The invention described in this application can also be extended to modulating the activity of other transcription factors such as the forkhead/winged helix transcription factor FOXP3 (Bennett et al., 2001; Fontenot et al., 2003; Hori et al., 2003; Wu et al., 2006; Zheng and Rudensky, 2007). FOXP3 is a key transcription factor critical to the development and function of regulator T cells (Tregs). Tregs are a special population of T cells required for suppressing the excessive activation of the immune system. Loss of function of FOXP3 by mutations and other mechanisms lead to fetal autoimmune diseases such as IPEX whereas enhanced expression of FOXP3 or its activity can confer suppression function. Elevated FOXP3 function can be beneficial in treating autoimmune diseases and transplant rejection while strategic down regulation of FOXP3 activity can be used to develop immune-based anti-tumor therapies (Zuo et al., 2007a; Zuo et al., 2007b). Thus, small molecules that bind FOXP3 and modulate its interaction with co-repressors and co-activators could have therapeutic application in autoimmune diseases, transplant rejection and cancer therapy.

Similarly to MEF2, the function of FOXP3 is tightly regulated by transcription co-regulators that include HAT (such as TIP60) and HDACs (including class I and class II HDACs) (Li et al., 2007). Thus, small molecules could be developed by methods described in this invention that binds FOXP3 and blocks its interaction with co-regulators including epigenetic regulators such as histone modifying enzymes and chromatin remodeling machines.

Similarly, targeting transcription co-regulators has also met its share of challenges.

Among the transcription co-regulators of transcription factors such as MEF2, class II HDACs are the best studied group.

Histone deacetylases (HDACs) (EC number 3.5.1) are a class of enzymes that remove acetyl groups from an ε-N-acetyl lysine amino acid on a histone. Its action is opposite to that of histone acetyltransferases (HATs). HDACs proteins are now also being referred to as lysine deacetylases (KDAC) to more precisely describe their activity rather than their target, which also includes numerous non-histone proteins.

As their name suggests, one of HDACs main functions is to remove acetyl groups from histone proteins. Histone proteins are the chief protein components of chromatin. They act as spools around which DNA winds and play an important role in gene regulation and DNA packaging. Histone proteins have tails that are normally positively charged due to the amine groups present on their lysine and arginine amino acids. These positive charges help the histone tails to interact with and bind to the negatively charged phosphate groups on the DNA backbone.

The association between DNA and histone acts as a vital control mechanism in regulating the ability of transcription factors to access DNA. Strong association between DNA and histones restricts access by transcription factors and therefore represses gene transcription (Morrison et al., 2007). Modification of histones or DNA can alter the strength of their association and thus modulate transcriptional activity (Morrison et al., 2007). Covalent addition of methyl, phosphate, or acetyl moieties has been shown to alter the nucleosome state and consequently affect transcription. Acetylation results from the addition of an acetyl group to the c-amino group of conserved N-terminal lysine residues on histones. Addition of acetyl groups to histones reduces the attractive force between positively charged histone proteins and the negatively charged DNA phosphate backbone, resulting in a more relaxed and accessible chromatin structure. HATs facilitate histone acetylation and are thus believed to be transcriptional activators. Conversely, HDACs serve to remove acetyl groups from histones and thereby repress transcription. Thus, it is the interplay between HATs and HDACs activity that primarily governs local chromatin structure and gene expression. HDACs alter global gene transcription through the deacetylation of chromatin. It should be noted that HDACs do not directly bind DNA sequence and require additional factors for target gene recognition (Morrison et al., 2007).

There are 4 recognized subtypes of HDAC proteins (class I-IV) based on function and DNA sequence similarities. The first two subtypes are considered “classical” HDACs whose activity are inhibited by trichostatin A (TSA). Class I HDACs includes HDACs 1, 2, 3 and 8, which are expressed ubiquitously (Zhang and Olsen, 2000). Class II HDACs has two subgroups, IIa that includes 4, 5, 7 and 9, and IIb that includes HDAC6 and HDAC10. Class IIa share a common structural organization, with carboxyl-terminal catalytic domain and an amino-terminal extension that mediates interactions with members of the myocyte enhancer factor 2 (MEF2) family of transcription factors. HDACs also differ in terms of their subcellular localization with class I generally found in the nucleus, class IIb are located mostly in the cytoplasm, while class IIa shuttle between the nucleus and the cytoplasm. Unlike class I HDACs, class IIa HDACs are tissue-restricted, with especially high levels of expression in heart, skeletal muscle, and brain (Zhang et al., 2002). Class III is a family of NAD⁺-dependent proteins not affected by TSA and class IV is considered an atypical category of its own. HDAC11 is grouped in class V.

Given the important roles that HDACs play in cellular processes, the medical applications of HDAC inhibitors (HDACi) is an intense area of research. However, many uses of HDACi in medicine were discovered without knowledge of the underlying mechanism. For example, in psychiatry and neurology, there is a long history of using valproic acid as mood stabilizers and anti-epileptics. The anticonvulsant property of valproic acid was accidentally discovered when it was being used as a vehicle for a number of other compounds that were being investigated as anticonvulsant. It was not until later that valproic acid was identified as a HDACi. In recent years, HDACi are being actively studied as a mitigator or treatment for neurodegenerative diseases. There has also been extensive effort to develop HDACi for cancer therapy. For example, Vorinostat (SAHA) has recently been approved for treatment of cutaneous T-cell lymphoma (CTCL). An alternative agent under clinical evaluation for CTCL is the cyclic depsipeptide natural product FK228 (Romidepsin) which is a potent inhibitor of class I HDACs. In addition, a clinical trial is studying the effects of valproic acid on the latent pools of HIV in infected persons. Despite the growing interest in the medicinal applications of HDACi, the exact mechanisms by which these compounds work are still not well understood. Thus, these efforts are largely guided by guesswork and trial-and-error experiments.

One particular problem with the use of HDACi is that most of the known small molecules that inhibit HDAC activity are designed to function by targeting the catalytic activity of HDACs. However, since the active site is a conserved feature shared by a large number of different HDAC isoforms, it is inherently difficult to identify isoform-selective HDACi. Therefore, most HDACi have low specificity and are incapable of specific targeting of any particular species of HDAC. For example, trichostatin A (TSA) is among the most potent reversible HDACi currently known, with an IC₅₀ in low nanomolar range. TSA with its hydroxamic acid group and its five-carbon atom linker to the phenyl group, has the optimal conformation to fit into the active site of HDAC (de Ruijter et al., 2003; Somoza et al., 2004). All HDACs are thought to be approximately equally sensitive to inhibition by TSA (de Ruijter et al., 2003).

A major impediment, therefore, for the discovery of small molecules that inhibit the function of HDACs and thereby modulate the activity of related transcription factors, is that the current state of the art is focused on the discovery and optimization of HDACi that are identified and evaluated through their ability to bind to the active site of the HDAC enzymes. Typically, these HDACi have the general structure R-L-Z, where R is a protein surface recognition group connected via a short fatty linker L to a Zn²⁺-chelating group Z that binds to the active site zinc atom. The most common chelating groups (Z) featured in the known HDACi are: hydroxamic acids (TSA, vorinostat, LAQ824, belinostat), thiol derivatives (FK228, largazole) or electrophilic ketones (trapoxin A). A potential drawback of such groups that bind tightly to metal cations like Zn²⁺ is that they may lack sufficient selectivity for a particular protein, resulting in various side effects.

Another class of known HDACi are the benzamides that feature an ortho-aminoanilide (2-aminoanilide) moiety, including MS-725, MGCD0103, pimeloylanilide ortho-aminoanilide (PAOA) and compound 106 (N¹-(2-aminophenyl)-N⁷-p-tolylheptanediamide) which was investigated as a potential therapeutic for neurodegenerative diseases including Friedreich's ataxia and Huntington disease (Chou et al., 2008; Herman et al., 2006; Paris et al., 2008; Rai et al., 2008; Thomas et al., 2008; Wong et al., 2003). Although the detailed molecular mechanism of action of this class of HDACi is not known, these molecules were postulated to involve binding of the o-aminoanilide group to the zinc atom of the HDAC active site, despite the lack of any direct evidence regarding such binding motif. Moreover, such molecules were found to exhibit biological activity implicating inhibition of HDAC function, even though other non-selective HDACi did not show similar activity. For example compound 106 was shown to be very active for the induction of frataxin, despite weak HDAC while closely related HDACi such as SAHA did not have this type of activity. Consequently, in light of the absence of a molecular mechanism for the actions of this class of compounds, the optimization of their therapeutic potential has been hampered.

Several additional factors resulting from the well-regulated biological roles of the various HDAC isoforms, impose further challenges for the conventional approaches to the design of HDACi. Experiments have shown that the amount of acetylated histones increases in the presence of HDACi. Yet, recruitment of HATs and HDACs by DNA-bound transcription factors results in the formation of multi-protein transcription regulatory complexes that confer cell type specificity and signal dependent regulation to arrays of subordinate genes. Using HDACi that inhibit HDACs indiscriminately is akin to throwing a monkey ranch into a complicated and delicately balanced machine. This explains the numerous undesirable side-effects observed in many of the trials involving HDACi.

The problems encountered in investigating medicinal uses of HDACi are also shared by researchers investigating epigenetic regulation. Epigenetic regulation is the establishment of inheritable gene expression patterns without permanently changing the DNA sequence. It has emerged as a key mechanism for regulating cellular function.

Alteration of epigenetic regulation is a hallmark of many diseases, especially cancer. Small molecules that are being developed as drugs in treating these diseases, typically found via phenotypic screening, act by modulating the epigenetic control of cellular process. As such, the fundamental mechanisms of epigenetic regulation is an area of intense interest. At the same time, the search for small molecule epigenetic regulators is becoming a very promising area for drug discovery.

Because epigenetic regulation is achieved largely through chemical modifications of chromatin structure by enzymes that act upon DNA (e.g. DNA cytosine methyltransferase) or proteins (e.g. HATs, HDACs, histone methylases, and histone demethylases), in this context, HDACs' role in regulating DNA transcription can be viewed as a component of epigenetic regulation. Similar to HDACi, the majority of current chemical modulators of epigenetic regulators inhibit these enzymes by binding to their catalytic site, which is often shared by multiple enzymes with distinct cellular roles.

Despite recent advances regarding the role of transcription factors such as MEF2, and its implication in several major diseases, it has not been possible to identify small molecules that are capable of modulating the function of MEF2. Such molecules would facilitate further advances in this field and can lead to new mechanism-based and structure-based therapeutic applications for MEF2-associated diseases, including inflammation, autoimmune diseases, neurodegenerative diseases, cancer, and cardiovascular disease.

Therefore, a general problem in this area of research has been the lack of small molecules that can target a specific epigenetic regulator enzyme or protein. A further problem has also been the lack of methods for the design, evaluation and optimization of such small molecules, in a manner that bestows the required selectivity without the associated drawbacks resulting from broad-spectrum activities across entire enzyme or protein classes. Such molecules will have important applications as molecular tools in studying the basic mechanism of epigenetic regulation as well as therapeutic agents for targeted therapeutic interventions.

SUMMARY OF THE INVENTION

Through extensive biochemical and structural studies (Guo et al., 2007; Han et al., 2005; Han et al., 2003), the inventors have unexpectedly discovered a unique structural feature of MEF2 that made it possible to modulate its activity using small molecules. This discovery lies at the core of the invention as it goes against conventional wisdom and opens up a new door of possibilities. Based on this unexpected discovery, inventors have devised a general strategy for modulating cellular processes by blocking the interactions between transcription factors and their co-factors via an interfacial inhibitor. Accordingly, this invention also provides methods for identifying, screening, assaying, and synthesizing small molecule modulators that are capable of binding to a site lying in the interfacial surface of the factor-cofactor complex, thereby, disrupting the formation of the complex.

Thus, this invention has solved the long standing problem of targeting the heretofore “undrugable” transcription factors such as MEF2.

With respect to the specificity problem faced by HDACi, this invention provides an alternative approach for the development of small molecule modulators of HDAC function. Rather than targeting the active site of a particular HDAC, the present invention targets the binding site of the HDAC with an associated transcription factor which is required for regulating transcription. Because different HDAC subtype will have different binding surface to different transcription factor, by targeting the interface of these protein-protein interactions, the specificity issue posed by the conservative active site is resolved.

In particular, the present invention targets the interaction between the transcription factor MEF2 and class IIa HDACs. The activity of MEF2 is controlled by class IIa HDACs that bind MEF2 on specific promoters to repress target gene expression (Potthoff and Olson, 2007). Some small molecule inhibitors of HDACs (HDACi) that are being developed for the treatment of a variety of cancers also show therapeutic potential in diseases where deregulation of MEF2 and HDACs activity is implicated, including cardiac hypertrophy, neurodegenerative disorders, and immune dysfunction (Morrison et al., 2007; Paris et al., 2008). These observations suggest that small molecules blocking class IIa HDAC:MEF2 interaction might offer similar clinical benefits as member-specific HDACi (Guo et al., 2007; Han et al., 2005; Han et al., 2003).

Class IIa HDACs function closely with MEF2 in muscle, neurons and T cells. Class IIa HDACs do not bind DNA but depend on its interaction with DNA-bound MEF2 for promoter targeting. This interaction is mediated by a short amphipathic helix conserved in class IIa HDACs but not other HDACs that binds to a hydrophobic groove on the MADS-box/MEF2 domain of MEF2 (Guo et al., 2007; Han et al., 2005; Han et al., 2003). Such a ligand/receptor like binding mechanism suggests that it might be possible to use small molecules to block the recruitment of class IIa HDACs to MEF2-specific promoters (Guo et al., 2007; Han et al., 2005; Han et al., 2003).

The invention is based on systematic structure and biochemical studies (Guo et al., 2007; Han et al., 2005; Han et al., 2003) suggesting that small molecules binding to MEF2 can modulate its activity in the recruitment of transcription co-regulator such as Cabin1, class IIa HADCS and p300/CBP. Most of the these co-regulators have intrinsic function to modify chromatin (e.g. HDACs, p300 and CBP) or the ability to recruit chromatin modifying enzymes and machinery (e.g. mSin3A that binds Cabin1, HP1, CtBP, 14-3-3 that binds class IIa HDACs). Thus, small molecules that bind MEF2 and modulate its interactions with other transcription co-regulators can serve as epigenetic modulators in tissues where MEF2 play key regulatory roles. These small molecules can therefore be used to treat diseases where the activity of MEF2-dependent gene expression is dysregulated. The dysregulation could result from genetic mutations of MEF2 and its associated factors, diminished or excessive signals leading to the reduced or overly activated MEF2 function, abnormal under- or over-expression of co-factors that bind and interact with MEF2. Potential clinical applications of the MEF2-binding small molecules include but not limited to diseases from the muscle, immune and nervous systems. In the muscle system are cardiac hypertrophy, muscle fiber type remodeling, and other muscle related diseases resulting from imbalanced MEF2 function. In the immune system are a variety of autoimmune diseases or immune deficiency that result from excessive or too little MEF2-dependent gene expression. MEF2-binding small molecules can also be used to manipulate the function of regulatory T cells and the overall immune response for preventing transplant rejection. Since MEF2-dependent gene expression is intimately linked to synapses remodeling and neuronal survival, MEF2-binding small molecules can also be used treat a variety of neurodegenerative diseases (e.g. Alzheimer's disease and Huntington disease etc), autism, psychiatric disorders, and impaired learning and memory that result from deregulated MEF2 function.

Because small molecule modulators of this invention operate by targeting binding sites located at the protein-protein interaction interface of the transcription factors and their co-factors, they are also referred to herein as interfacial inhibitors.

Having explained the basic principles of this invention, we now summarize the various aspects and embodiments of the invention below:

In a first aspect, the invention provides an assay for screening, identifying, or optimizing a candidate interfacial inhibitor. Assays in accordance with this aspect of the invention will generally include the steps of contacting the candidate interfacial inhibitor to an evaluating element comprising a molecular surface defined by a protein-protein interface, which includes beta strands S1, S2 and S3 and helix H2 of each MEF2 monomer and the short helix motif from Cabin1 and HDAC4 and HDAC 9. In some preferred embodiments, the evaluating element is operatively coupled with a reporting element that provides information about the candidate inhibitor. In a preferred embodiment, the assay is a cell-based luciferase assay that allow rapid and high throughput screen and optimization of small molecules that bind MEF2 and modulate its binding to transcription co-regulators. This assay is developed based on more than 10 years of structural and biochemical studies of MEF2 complexes by the inventor's laboratory. This invention claims that the protein-protein interface, first identified by crystallography studies, and further demonstrated by structure-guided mutation studies in the invention, could serve as the molecular basis for a highly specific and sensitive screen for MEF2-binding small molecules. In other embodiments, the evaluating element of the assay may be implemented with physical assays that include but are not limited to pull down, coimmunoprecipitation or fluorescence quenching and anisotropy or any in vitro binding assays and cell-based luciferase reporter assay, transgenic reporter assay that are based on the protein-protein interface indentified by this invention.

In a second aspect, this invention also provides compounds useful as epigenetic modulators of MEF2-dependent transcription in a variety of mammalian tissues that include but are not limited to muscle, immune and nervous systems. In some preferred embodiments, compounds in accordance with this aspect of the invention may include but are not limited to the previously published compounds (Chou et al., 2008; Herman et al., 2006; Paris et al., 2008; Rai et al., 2008; Thomas et al., 2008; Wong et al., 2003), pimeloylanilide orthoaminoanilide PAOA, and the commercially available homolog suberoylanilide orthoaminoanilide, or BML-210, as well as their structurally related derivatives.

In a third aspect, this invention also provides a molecular framework defined by the BML-210 binding site on MEF2 derived from the structural frame work established by the crystal structure of BML-210 bound to MEF2, as set forth in the crystal structure coordinates in Table 1. We co-crystallized BML-210 with a MEF2A (1-78) dimer bound to DNA. The crystals diffracted to 2.4 Å, and the structure was solved by molecular replacement using the MEF2A (1-78):DNA complex as the search model (Santelli and Richmond, 2000). BML-210 adopts an extended conformation to bind into the hydrophobic pocket of the MEF2 (FIG. 1 d). One end of the molecule, the phenylamide group, is surrounded by a number of hydrophobic residues including Leu66, Leu67, Thr70, Leu66′ (prime sign denote residues from the other monomer) and Thr70′. The amide group at this end is also in position to engage in hydrogen bonding interactions with Thr70 and Thr70′, respectively. At the other end of the BML-210, the ring-link electron density is in a more hydrophilic environment surrounded by Asn73, Gln56′, Asp61′ and Asp63′. This region correspond to the ortho-aminoanilide group. Here the ortho-aminoanilide moiety with its amide group make extensive van der waals contacts and potential hydrogen bonding interactions with residues of MEF2 (FIG. 1 d). The methylene groups of the octanediamide fit snugly between helix H2 of the two MEF2 molecules, making numerous contacts to the main chain and side chain of MEF2 residues, mostly of hydrophobic nature (FIG. 1 d). Based on the crystal structure of BML-210 bound to MEF2, we claim that the surface residues that contact or are close proximity to contact BML-210 and PAOA can be used to guide the design and screen of small molecules to MEF2 by experimental and computational based approaches. These residues include all the residues on strand S1, S2 and S3 and helix H2 of MEF2 that are exposed. This structural frame, coupled with the high throughput, specific and sensitive assay described in the present invention will allow rapid design and optimization MEF2-binding small molecules that include BML210 and PAOA derivatives and molecules based on novel molecular scaffolds. The crystal structure of BML-210 bound to MEF2 disclosed in this invention, in addition to defining the small molecule MEF2-binding site as described herein, it also reveals for the first time a likely binding site for the ortho-aminoanilide moiety present in BML-210 and in other benzamide-containing HDAC inhibitors. Notably, this binding site is different from the HDAC enzyme's active site as has been postulated previously for this class of HDAC inhibitors.

In a fourth aspect, the invention provides MEF2-binding small molecules useful for binding to the interfacial binding site defined by the molecular framework in the third aspect above. In one embodiment the provided molecules are MEF2-binding small molecules with a general structural formula derived from the identified binding site derived from the crystal structure of BML-210 bound to MEF2. The provided small molecules are designed to bind to the described structural fold and would potentially bind MEF2 with high affinity and selectivity. The compounds provided under this embodiment of the invention include compounds of the general formula R^(a)-L-R^(b) that bind to the MEF2 binding site, wherein:

-   -   R^(a) is a recognition group that binds to the hydrophobic         region of the MEF2 binding site selected from a group that         includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl,         alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—,         R^(c)R^(d)N(SO₂)—, wherein:         -   R^(c) and R^(d) are independently selected from a group             consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy,             aryl, heteroaryl, alkylamino, dialkylamino, arylamino or             heteroarylamino.     -   L is a linker consisting of a chain of up to 20 carbon atoms,         provided that up to three carbon atoms can be replaced with an         oxygen, nitrogen or sulfur atom, and further provided that it         can include substituents selected from a group consisting of:         -   alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy,             alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro     -   R^(b) is a recognition group that binds to the hydrophilic         region of the MEF2 binding site selected from a group that         includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl,         alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—,         R^(c)R^(d)N(SO₂), wherein:         -   R^(c) and R^(d) are independently selected from a group             consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy,             aryl, heteroaryl, alkylamino, dialkylamino, arylamino or             heteroarylamino.

In a preferred embodiment the provided compounds have the general structure Ar¹-L¹-L²-L³-Ar² wherein:

-   -   Ar¹ and Ar² are aromatic rings independently selected from a         group consisting of benzene, naphthalene, pyridine, pyrimidine,         pyrazine, quinoline, isoquinoline, pyrrole, furan, thiophene,         imidazole, pyrazole, oxazole, thiazole, isoxazole, indole,         benzimidazole, benzothiazole, benzoxazole, provided that the         aromatic ring may contain up to seven substituents selected from         a group consisting of: hydrogen, alkyl, alkenyl, alkynyl,         alkoxy, aryl, heteroaryl, amino, alkylamino, dialkylamino,         arylamino, heteroarylamino, hydroxy, or halo. The substituents         can also join together to form a ring of up to 12 atoms,     -   L¹ and L³ are linking groups independently selected from a group         consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O),         NR(C═O), S(═O) or —S(═O)₂—     -   L² is a linking group selected from a group consisting of a         chain of up to 10 carbon atoms, provided that up to three atoms         can be replaced with an oxygen, nitrogen or sulfur atom, and         further provided that these atoms can contain substituents         selected from a group consisting of:         -   alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy,             alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro

In a further preferred embodiment, the provided compounds have the general formula:

wherein:

-   -   R¹-R¹⁰ are independently selected from a group consisting of     -   L¹ and L³ are linking groups independently selected from a group         consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O),         NR(C═O), S(═O) or —S(═O)₂—     -   L² is a linking group selected from a group consisting of a         chain of up to 10 carbon atoms, provided that up to three atoms         can be replaced with an oxygen, nitrogen or sulfur atom, and         further provided that these atoms can contain substituents         selected from a group consisting of: alkyl, alkenyl, alkynyl,         aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto,         amido, sulfonamido, or fluoro

In a further preferred embodiment, the provided compounds are selected from the following list of compounds (FIG. 2)

These compounds showed a wide range of affinity in binding to MEF2 in vitro and in vivo, and could be used as lead to develop MEF2-based therapeutics in muscle, immune and nervous systems as mentioned above. The compounds indeed showed effect in promoting regulatory T cell functions in vitro and in mouse model, and are therefore potential drug leads for autoimmune diseases and preventing transplant rejection.

Methods for the preparation of the provided MEF2-binding molecules are also provided in this invention.

In a fifth aspect, the invention also provides compounds and compositions useful for treating diseases that result from deregulation of MEF2-dependent transcription. Compositions in accordance with this aspect of the invention will include one or more of a compound capable of blocking binding of MEF2 and its co-factors. The provided compounds and compositions can be used in therapeutic applications involving the modulation of epigenetic regulation associated with the interaction of transcription factors and their recruited histone-modifying enzymes. In particular, the provided MEF2-binding small molecules can be used to treat a variety of diseases resulting from deregulation of MEF2-dependent transcription, which include but not limited to cardiac hypertrophy, muscle fiber type remodeling, and other muscle-related diseases resulting from imbalanced MEF2 function; autoimmune diseases or immune deficiency that result from excessive or too little MEF2-dependent gene expression, and transplant rejection; a variety of neurodegenerative diseases (e.g. Alzheimer's disease and Huntington disease etc), autism, psychiatric disorders, and impaired learning and memory that result from deregulated MEF2 function. A further application of this embodiment of the invention involves small molecules that modulate the function of the FOXP3 transcription factor that can be used to treat a variety of diseases that result from deregulation of FOXP3-dependent transcription. These diseases include but not limited to autoimmune diseases, transplant rejection and cancer.

The sixth embodiment of this invention involves the preparation of the drug: MEF2 complex and its crystallization for structure determination. This protocol define the specific protein fragment of MEF2A (2-78) and the range of buffer conditions to obtain high quality of crystals of compounds bound to MEF2. This method of complex preparation and crystallization is essential for structural characterization of current and future small molecules bound to MEF2 and use the structure to guide the optimization of the lead compounds.

The above-mentioned and other features of this invention and the manner of obtaining and using them will become more apparent, and will be best understood, by reference to the following description, taken in conjunction with the accompanying drawings. The drawings depict only typical embodiments of the invention and do not therefore limit its scope

Other aspects and advantages of the invention will be apparent from the following description and the appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows three different depictions (a-c) of a crystal structure of MEF2 and the identified ligand binding site; (d) shown is BML-210 bound to MEF2A (1-78) at 2.4 Å resolution, including the amino acids involved in binding interactions with BML-210.

FIG. 2 shows the structures of BML-210, PAOA and related exemplary MEF2-binding molecules.

FIG. 3 shows a schematic diagram of MEF2-HDAC luciferase reporter assay for HDACi.

FIG. 4 shows normalized response for luciferase activity in MEF2-HDAC luciferase reporter assay 24 hrs after treatment with BML-210. The luciferase activity decreased in a dose dependent manner.

FIG. 5 (a) shows competitive inhibition of MEF2 binding to HDAC after incubation with BML-210 in Biacore assay; (b) Structural analysis showing that BML-210 and HDAC9 bind overlap regions on MEF2.

DETAILED DESCRIPTION

Having summarized the various aspects of this invention, we now describe in detail the various exemplary embodiments to further illustrate the invention.

Specific Interfacial Inhibitors of HDACs and Uses Thereof.

As mentioned above, what makes the study of epigenetic regulators challenging is the fact that there are a large number of enzyme isoforms, many of which have distinct functions. For example, among the four HDAC enzyme super families, class I (HDAC 1, 2, 3, and 8) and class II (HDAC 4, 5, 6, 7, 9, and 10) are the two major classes implicated in cancer. Although the unique function of each individual member can be studies by molecular biology approaches such as knockout or knockdown, their roles in drug-based therapy cannot be assessed because most current HDAC inhibitors target the catalytic domain common to most HDACs (class I and II). In fact, it is often observed that a given HDAC inhibitor induces what appears to be opposing effects in different cellular conditions, presumably by affecting the activity of different HDAC isoforms. Thus, the lack of isoform specificity of current HDACi presents a major barrier to rational mechanistic studies of drug effects and the individual function of specific HDACs. Also, it is not clear if it is more pharmacologically beneficial to inhibit a large number of HDACs or a small subset or even a specific member. It is possible that certain clinical applications (e.g. cancer therapy) may require the former, whereas others (e.g. neurodegeneration and inflammation) may benefit from the latter.

Currently available inhibitors of class I and class II HDACs can be grouped into six categories based on the key features of their chemical structures: (1) hydroxamic acids; (2) thiol-containing molecules; (3) electrophilic ketones; (4) short-chain fatty acids; (5) benzamides (ortho-aminoanilides); and (6) cyclic depsipeptides. While it is well established that some of these molecules, including hydroxamic acids, thiols, and electrophilic ketones, work by binding to the zinc ion of the HDAC active site, the inhibitory mechanism of the other categories are not well defined. Different HDAC inhibitors have shown different activities on different classes of HDACs. For example, while members of the hydroxamic acids category, such as TSA and SAHA, are potent inhibitors across the entire class I and class II HDACs, some members of the benzamide family (e.g. pimeloylanilide ortho-aminoanilide (PAOA), MS-275, CI-994, MGCD-0103), and the cyclic peptide family (e.g. FK228), showed modest selectivity toward certain HDAC members or subclasses. However, because of the general lack of understanding of the molecular mechanisms of HDAC inhibitors, how this selectivity is achieved is not clear. Consequently, the empirical observations of selectivity in some HDAC inhibitors could not guide rational design of subtype-specific HDAC inhibitors. While crystal structures of the catalytic domain of several class I (HDAC8) and class II (HDAC4 and HDAC7) members and their complexes with different inhibitors have been solved, these structures and the structure-based sequence-alignments of class I and class II HDACs suggest that the active site is highly conserved and show only minor differences in the surrounding region. Therefore, they also fail to provide any insights with regard to potential mechanisms of selectivity. Given this background, rational design of subtype-specific inhibitors against the highly conserved catalytic domain is widely considered to be highly challenging.

Observing that HDACs often exist in large multi-protein complexes with specific co-regulators and other chromatin modifying enzymes, inventors of this invention postulated that a mechanism-based approach may offer a better pathway to identifying and optimizing novel HDAC-based small molecule epigenetic regulators. That is, instead of targeting the active site of the enzyme as dictated by conventional approaches of drug design, one would develop small-molecules targeting the protein-protein interactions between HDACs and their relevant functional partners.

Accordingly, in one aspect, this invention provides a method of modulating HDAC function by blocking the binding of HDAC to an associated transcription factor. In general, methods according to this aspect of the invention will have the steps of: contacting the transcription factor with interfacial inhibitor, wherein the interfacial inhibitor is capable of selectively binding to a site within the interfacial surface between the transcription factor and HDAC, thereby preventing this HDAC from performing its catalytic activity at protein sites that are located in the vicinity of the DNA-binding site of the transcription factor.

The HDAC may be any HDAC isoform from a classical HDAC or a subset thereof. Exemplary HDAC may include HDAC 4, 5, 6, 7, 9 and 10, or any subset thereof. In a preferred embodiment, the HDAC is a class IIa HDACs, and in a further preferred embodiment the HDAC is either HDAC4 or HDAC9.

The transcription factor may be any transcription factor known to bind to the HDAC. Exemplary transcription factors may include MEF2, FOXP3, GATA3, and Cabin1 but are not limited thereto. In a preferred embodiment, the transcription factor is MEF2.

The interfacial inhibitor may be a small molecule.

Methods described herein above may be used in a research setting for obtaining information regarding the function and mechanisms of a HDACs and the counterpart transcription factor in vivo or in vitro. They may also be used in a clinical setting for treating diseases.

Diseases that may be treated with methods of this invention are generally those involving cardiac hypertrophy, muscle fiber type remodeling, and other muscle-related diseases resulting from imbalanced MEF2 function; autoimmune diseases or immune deficiency that result from excessive or too little MEF2-dependent gene expression, and transplant rejection; a variety of neurodegenerative diseases (e.g. Friedrich's ataxia, Alzheimer's disease and Huntington disease etc), autism, psychiatric disorders, and impaired learning and memory that result from deregulated MEF2 function. Exemplary diseases may include neurodegenerative diseases, heart diseases, autoimmune diseases, inflammation, and cancer, but are not limited thereto.

When used in a clinical setting, methods in accordance with this aspect of the invention will include the general steps of: administering to a patient a pharmaceutically effective amount of a blocking agent, in which the blocking agent is capable of blocking the binding of a HDAC to a transcription factor.

When used in a different clinical setting, methods in accordance with this aspect of the invention will include the general steps of: administering to a patient a pharmaceutically effective amount of a blocking agent, in which the blocking agent is capable of blocking the binding of a Cabin1 to MEF2. Cabin1 is a transcription co-repressor of calcineurin-dependent transcription program. It is highly expressed in T cells and neuronal cells.

When used in yet a different clinical setting, methods in accordance with this aspect of the invention will include the general steps of: administering to a patient a pharmaceutically effective amount of a blocking agent, in which the blocking agent is capable of blocking the binding of a p300 to MEF2.

When used in yet a different clinical setting, methods in accordance with this aspect of the invention will include the general steps of: administering to a patient a pharmaceutically effective amount of a blocking agent, in which the blocking agent is capable of blocking the binding of a CBP to MEF2.

In a more general setting, methods in accordance with this aspect of the invention will include the general steps of: administering to a patient a pharmaceutically effective amount of a blocking agent, in which the blocking agent is capable of blocking the binding of any transcription co-regulators that bind MEF2.

As set forth above, the HDAC may be any classical HDAC or a subset thereof. The blocking agent may be a small molecule, a helical peptidomimetic, or a combination thereof, so long as the blocking agent is capable of selectively binding to a site located on the interfacial surface between the HDAC and the transcription factor. In a preferred embodiment, the transcription factor is MEF2.

Methods and Tools for Developing Interfacial Inhibitors

In another aspect, this invention also provides an assay for identifying an interfacial inhibitor capable of binding to an interfacial site between HDAC and a transcription factor so as to block the interactions thereof.

Assays in accordance with this aspect of the invention will generally have the steps of introducing a test compound to an evaluation element, wherein said evaluation element comprises an interfacial binding site on a MEF2 dimer defined by the interface between a first group of structural elements on the MEF2 dimer and a second group of structural elements. The first group of structural elements include the beta strands S1, S2, S3, and the helix H2 of each of the MEF2 monomer (The secondary structural elements and corresponding residue ranges are as described in Han et al., Nature 2003). The second group include the short helix, motif from Cabin1, HDAC4, HDAC9, HDAC5, HDAC7, p300 and CBF. The evaluation element may also be operatively coupled with a reporter element for reporting information related to the binding or non-binding of the test compound.

In a preferred embodiment, there is disclosed herein a two-hybrid system based assay includes a binding domain fused with a bait, an activating domain fused with a prey, and a reporter gene; and determining a reporter signal level. The binding domain comprises a MEF2D fused with GAL4 DNA (GAL4-MEF2); the activating domain comprises MEF2 binding motif of HDAC4 fused with VP-16 (HDAC4-VP16). The reporter gene is a GAL4-driven reporter plasmid (GAL4Luc), all hosted in a cell host.

This preferred embodiment of this invention is a cell-based luciferase assay that allows rapid and high throughput screening and optimization of small molecules that bind to a transcription factor such as MEF2 and modulate its binding to transcription co-regulators. The assay is developed based on more than 10 years of structural and biochemical studies of MEF2 complexes by the inventor's laboratory. This exemplary embodiment based that the protein-protein interface, first identified by crystallography studies, and further demonstrated by structure-guided mutation studies in the invention, could serve as the molecular basis for a highly specific and sensitive screen for MEF2-binding small molecules.

Any assay that based on this protein-protein interface, which include beta strands S1, S2 and S3 and helix H2 of each MEF2 monomer and the short helix motif from Cabin1 and HDAC4 and HDAC 9 are considered to be within the scope of this invention. Other exemplary assay implementations may include any physical assay techniques such as, but not limited to, pull-down, co-immunoprecipitation; fluorescence-based binding assays and functional assays including, but not limited to, luciferase reporter assay, and transgenic reporter assay that are based on the protein-protein interface indentified by this invention.

In particular, in order to establish if a provided compound can indeed disrupt the binding of class IIa HDAC inside cells, several types of assays can be used, including the Chromatin Immunoprecipitation (ChIP) assay. HDAC4 plasmid construct is transiently transfected into Hela Cells. HDAC4 occupation on MEF2 mediated promoters are detected by ChIP using appropriate specific antibodies and PCR primers in the presence of the tested compound and buffer control. A fluorescence imaging based method as an alternative approach to ChIP analysis can also be used. GFP-fused MEF2C and HDAC4 is transfected into HeLa or C2C12 cells to study their interaction. When expressed alone, GFP-HDAC4 localizes in the cytoplasm in a diffusive manner, whereas GFP-MEF2 localizes in the nucleus, also in a diffusive pattern. When co-expressed, HDAC4 and MEF2 form punctate bodies inside the nucleus. Although the nature of these punctate nuclear bodies is unknown, their formation is apparently dependent on MEF2:HDAC4 interaction, as a HDAC4 mutant lacking a functional MEF2-binding motif fails to target MEF2 to nuclear bodies. Finally, a genome-wide analysis of MEF2 target genes by mRNA profiling (microarray) and binding location (ChIP-on-chip) can further facilitate this method, by selecting well-known MEF2 target genes that show large responses to MEF2-dependent repression or activation in the resting or activated (e.g. with calcium signal turned on) state. Using this method it can be established if these genes are potentially regulated by class II HDACs or other MEF2 co-repressors (e.g. Cabin1) by detecting the promoter presence of class IIa HDAC using ChIP and by monitoring expression changes upon drug treatment or after siRNA knockdown of HDAC4, 5, 7 or 9 (expression changes due to siRNA are evaluated first). Overall this method can be used to evaluate a compound at a genome-wide level by analyzing gene expression using microarray and by detecting genome-wide binding of class IIa HDACs in the presence of various concentrations of the provided compound.

To facilitate performing the assay, this invention also provides a high throughput, highly sensitive and specific screen platform for searching MEF2-binding small molecules. This platform comprises stably transformed cell lines containing the GAL4-driven reporter plasmid (GAL4Luc), MEF2D fused with GAL4 DNA-binding domain (GAL4-MEF2), the MEF2-binding motif of HDAC4 fused with VP-16 (HDAC4-VP16), GAL4 DNA-binding domain fused with VP-16 (positive control) and various compounds as negative and positive controls. A kit consistent of the above stable cell lines, plasmids, and control compounds can be made for the screen by users searching for new MEF2-binding molecules and for optimizing existing leading compounds. By switching MEF2D to MEF2A, MEF2B and MEF2C, one can also use this method to search for compounds that bind selectively to an isoform of the MEF2 family. Such compounds can be used to study the function and involvement of specific MEF2 family members in diseases and can be employed in the development of diagnostic agents and for the identification of more specific therapeutic agents for MEF2-associated diseases.

In yet another aspect, the invention also provides a method for identifying a subtype-specific HDAC inhibitor/modulator by targeting their regulatory and functional complexes. Methods in accordance with this aspect of the invention generally includes the steps of: (1) solving the structure or substructure that contains functionally important interfaces; (2) applying docking analysis to the solved structures by computationally docking test molecules selected from existing or new potential HDAC inhibitors; (3) developing an assay for screening compounds that can disrupt the protein-protein interactions between the HDAC complex of interest; (4) characterizing the compound identified in step (3); (5) optimizing the compound computationally; and (6) synthesizing the optimized compound and validating the compound using the assay of step (3).

For step 1, the structure can be solved by molecular replacement using existing structure as the search model. If necessary, experimental phases can be obtained MAD or MIR. For step 2, docking can be performed using standard package such as AutoDock. Step 3 is as described above and will most be based on mammalian two-hybrid assay. The rest of the steps will depend on the nature of the compounds using methods known in the art.

In still another aspect, the invention also provides compounds useful as blocking agents for blocking the binding between a HDAC and a transcription factor. The HDAC may be any classical HDAC or a subset thereof. The transcription factor may be any transcription factor known to bind to HDAC, including but not limited to MEF2, FOXP3 and GATA3.

In a preferred embodiment, the transcription factor is MEF2.

Compounds according to this aspect of the invention include small organic molecules and helical peptidomimetics.

MEF2-binding small molecules can be identified using the method provided herein, by utilizing the disclosed MEF2 binding site as a guide. The provided small molecules have a general structural formula derived from the identified binding site revealed from the crystal structure of BML-210 bound to MEF2. The provided small molecules are designed to bind to the described structural fold and would potentially bind MEF2 with high affinity and selectivity. In order to identify more potent and selective compounds using this approach, methods known in the art can be utilized, including but not limited to: computer-aided structure-based design combined with in-silico screening, combinatorial library design combined with high-throughput screening, and fragment-based drug discovery for lead identification followed by lead optimization.

In a preferred embodiment, the compounds provided under this invention include compounds that bind to the MEF2 binding site with the general formula:

R^(a)-L-R^(b), wherein:

-   -   R^(a) is a recognition group that binds to the hydrophobic         region of the MEF2 binding site selected from a group that         includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl,         alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—,         R^(c)R^(d)N(SO₂), wherein:         -   R^(c) and R^(d) are independently selected from a group             consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy,             aryl, heteroaryl, alkylamino, dialkylamino, arylamino or             heteroarylamino.     -   L is a linker consisting of a chain of up to 20 carbon atoms,         provided that up to three carbon atoms can be replaced with an         oxygen, nitrogen or sulfur atom, and further provided that it         can include substituents selected from a group consisting of:         -   alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy,             alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro;     -   R^(b) is a recognition group that binds to the hydrophilic         region of the MEF2 binding site selected from a group that         includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl,         alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—,         R^(C)R^(d)N(SO₂), wherein:         -   R^(c) and R^(d) are independently selected from a group             consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy,             aryl, heteroaryl, alkylamino, dialkylamino, arylamino or             heteroarylamino.

In a preferred embodiment the provided compounds have the general structure Ar¹-L¹-L²-L³-Ar² wherein:

-   -   Ar¹ and Ar² are aromatic rings independently selected from a         group consisting of benzene, naphthalene, pyridine, pyrimidine,         pyrazine, quinoline, isoquinoline, pyrrole, furan, thiophene,         imidazole, pyrazole, oxazole, thiazole, isoxazole, indole,         benzimidazole, benzothiazole, benzoxazole, provided that the         aromatic ring may contain up to seven substituents selected from         a group consisting of: hydrogen, alkyl, alkenyl, alkynyl,         alkoxy, aryl, heteroaryl, amino, alkylamino, dialkylamino,         arylamino, heteroarylamino, hydroxy, or halo. The substituents         can also join together to form a ring of up to 12 atoms,     -   L¹ and L³ are linking groups independently selected from a group         consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O),         NR(C═O), S(═O) or —S(═O)₂—     -   L² is a linking group selected from a group consisting of a         chain of up to 10 carbon atoms, provided that up to three atoms         can be replaced with an oxygen, nitrogen or sulfur atom, and         further provided that these atoms can contain substituents         selected from a group consisting of:         -   alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy,             alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro

In a further preferred embodiment, the provided compounds have the general formula:

wherein:

-   -   R¹-R¹⁰ are independently selected from a group consisting of     -   L¹ and L³ are linking groups independently selected from a group         consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O),         NR(C═O), S(═O) or —S(═O)₂—     -   L² is a linking group selected from a group consisting of a         chain of up to 10 carbon atoms, provided that up to three atoms         can be replaced with an oxygen, nitrogen or sulfur atom, and         further provided that these atoms can contain substituents         selected from a group consisting of: alkyl, alkenyl, alkynyl,         aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto,         amido, sulfonamido, or fluoro

In a further preferred embodiment, the provided compounds are selected from the following list of compounds (FIG. 2)

To further facilitate a complete understanding of the various aspects and ramifications of this invention, the following illustrative examples are provided.

EXAMPLES Example 1 Strategy for Identifying Subtype-Specific HDAC Inhibitors/Modulators

This invention provides a novel strategy for identifying lead compounds that may act as subtype-specific HDAC inhibitor/modulators. The strategy consists of several iterative steps:

Step 1: for a given HDAC complex of interest, the structure or substructure of the HDAC bound to its associated regulatory protein is solved or its structure or substructure that contains functionally important interfaces is obtained.

Step 2: the structure is used for docking analysis of existing or new potential HDAC inhibitors that may bind the protein-protein interface. The virtual screen will be guided by functional data such as if the HDAC inhibitor showed effect in cellular processes involving the target HDAC complex and if the HDAC inhibitor seems to act through mechanisms other than active site inhibition.

Step 3: the structure and related biochemical information is also used to guide the development of assays that can be used to screen compounds that can disrupt the intended protein-protein interface.

Step 4: once such leads are found, their complexes with the protein target is characterized using the structural study system established in Step1.

Step 5: the structural information, in combination with relevant chemistry methodologies is used to guide the design of analogs that can bind the target protein with higher affinity and specificity. The methods used are similar to that of Step 2.

Step 6: the designed analogs are synthesized and analyzed by assays established in Step 3. Finally, the optimized compounds are used for in vivo studies to test if they can mimic the effects of the parent compound but with higher potency and less non-specific/side effects.

Utilizing the above mechanism-based approach, inventors have demonstrated that a previous known HDAC inhibitor, PAOA, was identified as a lead compound that can specifically disrupt the function of class IIa HDACs by serving as a MEF2 inhibitor (MEF21). Moreover, representative structural analogs of PAOA were also designed, synthesized and evaluated with the method described herein, and several more potent MEF21 were identified (FIG. 2), thereby demonstrating further aspects of this approach.

Example 2 Uses of Subtype-Specific HDAC Inhibitors in Therapeutic Applications

Class IIa HDACs play crucial roles in neuronal survival/synapse formation, T cell selection/activation, and muscle remodeling. Dysregulation of these activities are implicated in a number of diseases, including neurodegeneration, inflammation and cardiac hypertrophy. Some HDACi developed for cancer therapy showed beneficial effects against these disorders. Although the non-specific nature of these HDAC inhibitors prevent their clinical applications in these diseases, these observations raise an intriguing question whether the observed therapeutic effects were related to class IIa HDACs, and whether selected disruption of class IIa HDAC function could be a viable strategy for treating these diseases. To address these questions, small molecules that can specifically disrupt the function of class IIa HDACs are needed.

Based on the known cellular functions of MEF2 and class IIa HDACs and the effects of some HDAC inhibitors in muscle, immune and neuronal systems, we propose methods and compounds of this invention could be used to treat cardiac hypertrophy, muscle fiber type remodeling, and other muscle-related diseases resulting from imbalanced MEF2 function; autoimmune diseases or immune deficiency that result from excessive or too little MEF2-dependent gene expression, and transplant rejection; a variety of neurodegenerative diseases (e.g. Friedrich's ataxia, Alzheimer's disease and Huntington disease etc), autism, psychiatric disorders, and impaired learning and memory that result from deregulated MEF2 function.

The MEF2-binding molecules developed for treating various human diseases mentioned above could be administered orally, intramuscular, intraperitoneal, subcutaneous, intravenous injections. Other delivery methods are also possible, and the exact protocol will depend on the conditions that are being treated. The dose could also vary according to specific clinical applications. But the standard assays at which the compound shows effect in vitro is around 0.1-10 μM in vitro and 1-10 mg per KG of body mass in animal model studies.

Preferred compounds provided under this invention shown in FIG. 2 exhibited a wide range of affinity in binding to MEF2 in vitro and in vivo, and could serve as lead compounds to develop MEF2-based therapeutics in muscle, immune and nervous systems as mentioned above. The compounds indeed showed effect in promoting regulatory T cell functions in vitro and in mouse model, and are therefore potential drug leads for autoimmune diseases and preventing transplant rejection. For example, the MEF2-binding molecule NKL30 at 0.15 μM greatly enhanced regulatory T cell function as evident by the enhanced suppression activity in vivo. In an mouse model of homeostatic proliferation assay, the compound at 1 mg/KG body mass administered by intravenous injection also greatly enhanced the Treg function in vivo. These data strongly suggest that MEF2-binding molecules provided by this invention could be used to treat autoimmune diseases and for preventing transplant rejection.

Example 3 Targeting Class IIa HDACs for Functional Modulation

Compared with other HDACs, the class IIa family is unique in several aspects of function and regulation. First, class IIa HDACs are selectively expressed in muscle, brain and T cells, consistent with their functions in these tissues. Second, the activity of class IIa HDACs is tightly regulated by the calcium signal, a predominant second messenger in tissues where class IIa HDACs are expressed. Third, class II HDACs contain a large regulatory domain N-terminal to the catalytic domain, which confers unique properties to this subclass of HDACs. The N-terminal regulatory region contains domains and motifs that interact with a variety of proteins, including those regulating the calcium responsiveness of class II HDACs, such as CaM, CaMK and 14-3-3, and those targeting class II HDACs to specific promoters such as MEF2 and BCL-6, and other epigenetic regulators and effectors such as class I HDACs, CtBP and HP-1 that function cooperatively with class IIa HDACs. The structures of a number of these complexes are investigated as potential targets for specific disruption.

Among the many complexes involved in the regulation and function of class IIa HDACs, the best characterized is the MEF2 complex in terms of biochemistry and structure. MEF2 is a family of sequence-specific transcription factors (MEF2A-D) that has the same expression pattern as class IIa HDACs and is also implicated in neurodegeneration, inflammation and cardiac diseases. The MEF2 family of transcription factors share a highly conserved N-terminal region, referred to as the MADS-box/MEF2S domain, that mediates DNA binding, dimerization and protein-protein interactions with a variety of transcription factors and co-regulators. Class IIa HDACs do not bind DNA but depend on interaction with MEF2 to target specific chromatin regions for deacetylation. Blocking this interaction is selected as a potential way to disrupt the function of class IIa HDACs.

The interaction between class IIa HDACs and MEF2 has been the subject of extensive functional and biochemical analyses, which reveal that a short sequence motif (MEF2-binding motif) conserved in class IIa HDACs and the MADS-box/MEF2S domain of MEF2 are necessary and sufficient for their binding. Systematic structural and biophysical studies were conducted on the interaction between MEF2 and class IIa HDACs and a related transcription repression (Cabin1) that contain a similar MEF2-binding motif. The crystal structures reveal that the MEF2-binding motif adopts a short amphipathic helix structure to bind a hydrophobic groove on the MADS-box/MEF2 domain of MEF2. Such a ligand/receptor like binding mechanism suggests that it might be possible to use small molecules to block the recruitment of class IIa HDACs to MEF2-specific promoters (refs Han Nature and 2005).

Example 4 Development of a Sub-Class Specific HDAC Inhibition Assay

A series of MEF2-dependent luciferase reporter assays with transiently transfected MEF2D, HDAC4 and the co-activator p300 were used initially to screen various compounds. But these assays gave weak signal and high frequency of false positives, probably due to the complex transcription activation mechanisms of MEF2 and interference from endogenous factors. Through these observations, it was discovered that a highly sensitive and specific assay that can recapitulate the molecular interaction between HDAC4 and MEF2 inside cells is essential. To solve this problem, the inventors devised a mammalian two-hybrid system that is capable of detecting the interaction between HDAC4 and MEF2D with minimal interference from endogenous factors (FIG. 3).

In this assay system, MEF2D is fused with GAL4 DNA binding domain (GAL4-MEF2D) and the MEF2-binding motif of HDAC4 (aa 155-220) fused with VP-16 (HDAC4-VP16). Preliminary analysis showed that Hela Cells transiently transfected with both constructs and the GAL4-driven reporter plasmid (GAL4Luc) produced a strong signal comparable to that generated by the positive control of GAL4-VP16, whereas a MEF2D mutant Leu67Asp (L67D) that is previously shown to be defective in binding to HDAC4 failed to activate the reporter (data not shown). Protein expression levels in all luciferase reporter assays were confirmed by western blot.

Taking advantage of the structural insights, in addition to the MEF2D L67D mutant mentioned above, we introduced a number mutations in HDAC4 that had been previously shown to disrupt HDAC4:MEF2 interaction in vitro. These mutations also diminished the luciferase signal in the cell-based assay (FIG. 3 b). Most interestingly, mutation of Val180Lys on HDCA4, which weakened the binding of MEF2 by ˜60% in vitro (Kd of MEF2 binding by the wild type and the mutant HDAC4 are 0.47 μM and 0.81 μM, respectively), partially reduced the luciferase signal in the cell-based assay (FIG. 3 b). These observations demonstrate that the signal from the mammalian two-hybrid assay correlates very well with the molecular interaction between HDAC4 and MEF2. These results not only provide further support for the structural model of the HDAC4:MEF2 interaction but also establish a sensitive and specific method for detecting the HADC4:MEF2 interaction inside the cells.

Example 5 Identifying Selective Inhibitors of the MEF2/HDAC Interaction

To reduce the complexity of the screening, the vast amount of functional data on existing HDAC inhibitors was utilized. Although most of the these inhibitors target the catalytic domain, some of the compounds discovered through the cell based histone acetylation assays may affect other aspects of HDAC function, including the binding of class IIa HDACs to MEF2. With this in mind, we performed virtual screen (3D docking) against a small molecule database using a pharmacophore model derived from the crystal structure of the HDAC9:MEF2 complex. Although this search did not yield a novel target, it did show that the hydrophobic pocket of MEF2 prefers compounds with two aromatic rings connected by a linker of certain length. This result is consistent with crystallographic analysis showing that the MEF2 dimer contains two symmetry-related sites that can bind a phenylalanine from HDAC9 (refs Han et Nature and JMB). We therefore searched for known HDAC inhibitors that bear such structural features and tested their effect on HDAC4:MEF2 interaction using the mammalian two-hybrid assay.

Screening a pool of selected HDAC inhibitors using the mammalian two-hybrid assay revealed that PAOA (FIG. 2), a previously studied compound inhibited the reporter signal in a dose dependent manner (FIG. 4). PAOA did not affect the expression of HDAC4-VP16 but reduced the reporter signal driven by GAL4-VP16 by 5.6 fold at 10 μM (data not shown), indicating non-specific inhibition by this compound on the expression of luciferase activity under our experimental conditions. However, the same concentration of PAOA decreased the reporter signal driven by GAL4-MEF2D and HDAC4-VP16 by about 26 fold, suggesting that PAOA have specific effect on disrupting the HDAC4:MEF2 interaction beyond its general inhibitory effect. By contrast, trichostatin A (TSA), a potent HDAC inhibitor that targets the zinc active site, showed similar inhibitory effect on the reporter signals driven by GAL4-VP16 and GAL4-MEF2D/HDAC4-VP16 (data not shown). These results suggest that PAOA but not TSA can disrupt the interaction between HDAC4 and MEF2D.

The IC50 of PAOA on HDAC4:MEF2 interaction is around 5 μM based on the mammalian two-hybrid assay, similar to that determined using histone acetylation inhibition assay. The Kd for HDAC4 binding to MEF2 was previously determined to be 0.47 μM. If we assume the equilibrium concentration of HDAC4 is ˜0.5 μM under our assay condition, the Kd for the binding of PAOA to MEF2 is estimated to be 5 μM. However, the estimated Kd could be larger if the free HDAC4 concentration is lower in the cell-based assay.

Whether PAOA binds MEF2 competitively with HDAC4 was also assessed in vitro using surface Plasmon resonance (SPR) on Biacore T-100. Here HDAC4 (aa 155-220) was immobilized on a CM5 sensor chip and purified MEF2A (1-95) was used as the analyte. The binding of MEF2A to HDAC4 at various concentrations generated a series of well-defined sensorgrams (data not shown). MEF2A incubated with increasing concentrations of PAOA showed dose dependent decrease of binding to the immobilized HDAC4 (FIG. 5). Analysis of the Biacore data indicates that the competitive binding reaction is complex, whereas direct binding of BML-210 to MEF2 was beyond the detection limit of the instrument. These technical limitations made it difficult to obtain a quantitative binding constant. Nevertheless, the preliminary data suggest that BML-210 indeed bind MEF2 competitively with HDAC4 in vitro.

PAOA was originally discovered as part of a group of compounds that selectively induce acetylation of histone but not tubulin, presumably through inhibition of HDACs other than HDAC6, a tubulin-specific HDAC. PAOA binds MEF2 competitively with HDAC4 in vitro. The inserts on the right illustrate the assay by Biacore. HDAC4: red helix; MEF2: green cross. deacetylase. Although the molecular basis of this selectivity is not known, it is noteworthy that HDAC6, which belongs to the class IIb subfamily, does not have the MEF2-binding motif conserved in class IIa and does seem to require MEF2 for function. PAOA and its derivatives have been recently shown to enhance the expression of frataxin in Friedreich's ataxia. Although the mechanism seems to involve induced histone acetylation, more potent but less specific HDAC inhibitors such as TSA and SAHA showed no effect on frataxin expression despite being able to induce higher level total histone acetylation in cells than PAOA. These observations suggest that PAOA and its derivatives possess a unique function to inhibit a specific HDAC or HDAC complex involved in frataxin silencing. Furthermore, the molecular basis for the action of PAOA can be further clarified with the crystal structure of BML-210 bound to MEF2 disclosed in this invention. In addition to defining the small molecule MEF2-binding site as described herein, this structure also reveals for the first time a likely binding site for the ortho-aminoanilide moiety present in BML-210, as well as PAOA and in other benzamide-containing HDAC inhibitors. Notably, this binding site is different from the HDAC enzyme's active site as has been postulated previously for this class of HDAC inhibitors.

Example 5 Preparation of Complexes of BML-210 Bound to MEF2 on DNA and the Crystals of the BML-210:MEF2:DNA Complex and the Atomic Details of the Complex Structure

In order to characterize the detailed interaction of BML-210 bound to MEF2 and use the structural information to guide the design of more potent MEF2 binding molecules, we have determined the crystal structure of the BML-210 bound to MEF2 on DNA. The gene coding MEF2A1-78 was created by PCR amplification from MEF2AFL and cloning into the pET30b expression vector. Protein was expressed in E. coli strain BL21(DE3)pLysS, 25C, overnight and was purified by successive chromatographic steps on Sp-Sepharose, and gel filtration run at 4 C in 250 mM NaCl, 10 mM Hepes (pH7.6), 1 mM EDTA, 1 mM DTT to give a final yield of 0.6 mg/l. Oligonucleotides (Santelli and Richmond, 2000) were purchased from IDT DNA technologies, purified using MonoQ FPLC column followed by dialysis, lyophylization and annealing using thermal cycler.

1/10^(th) protein sample volume of 10 mM BML 210 was added to the protein samples at 0.5 mg/ml and concentrated to approximately 17 mg/ml (0.9 mM). and DNA duplex was added at 1:1 ratio prior to setting trays (10% DMSO end concentration). Plate like crystals were obtained by hanging drop vapor diffusion conditions at 18C using 24% PEG4000, 140 mM NaCl, 5 mM MgCl₂, 10 mM CaCl₂, 0.004% NaN₃, 3.3% glycerol, 50 mM TrisHCl (pH 5.8-pH8.18). Crystals with drug density were obtained at pH 8.18. The crystal diffracted to 2.4 Å resolution and belongs to space group P1 (a=41.567 Å, b=61.622 Å c=61.478 Å α=114.12° β=89.99° γ=89.95°. The structure is solved by molecular replacement using 1TQE.pdb as search model (refs Richmond 2000). The final model has an Rfree of 26% and Rw of 23%. The coordinates are attached (11.1_(—)001_nr_nh_bm1.pdb).

Example 6 Lead Optimization Using Structure-Guided Design and Chemical Methodologies

Most HDAC inhibitors discovered by functional screen have modest potency with IC50 in the micromolar or even millimolar range. Lead optimization is typically done by systematic modifications of the chemical structure and structure-activity relationships (SAR) studies. However, without knowing the target and the detailed binding interactions between the compound and its target, such an empirical approach is often labor intensive and of limited effectiveness. This is in fact the case for PAOA where a series of analogs were synthesized to search for more potent compounds that may be used for treating Friedreich's ataxia. Although some PAOA analogs did show higher activity than the parent compound, the effect was very modest and the mechanism of improvement was not clear.

Remarkably, the ability by which these PAOA derivatives activate frataxin expression did not correlate with their HDAC inhibition activity. For example, some of the derivatives were very weak in histone deacetylation inhibition assay and yet very active in frataxin induction. Our preliminary findings that PAOA binds MEF2 and block the recruitment of class IIa HDACs provide a potential molecular mechanism for these intriguing results. Class IIa HDAC can repress transcription independent of the deacetylase activity. For example, a naturally occurring splicing variant of HDAC9 that lacks the entire C-terminal catalytic domain, also known as MITR, is a potent transcription repressor of MEF2-dependent gene expression, presumably by recruiting other epigenetic effectors such as HP1 and CtBP. In this sense, small molecule inhibitors that target the catalytic domain of class IIa HDACs cannot eliminate the full epigenetic silencing potential of these proteins, which may explain the ineffectiveness of TSA and SAHA in reactivating frataxin expression. PAOA, on the other hand, can block the recruitment of HDAC activity and other transcription repressors together. Although MEF2 is also involved in gene activation by recruiting transcription activators such as CBP/p300, current data suggest that the main effect of PAOA on MEF2 dependent gene expression is alleviating the silencing effect of class IIa HDACs and other transcription repressors.

By relying on the above analysis and the disclosed structure of BML-210:MEF2:DNA, and by employing docking solutions of PAOA to MEF2A it is shown that this drug molecule can fit preferably into the experimentally observed electron density, demonstrating the relative effectiveness of the ICM-Docking protocol (Molsoft L.L.C) for the design of new PAOA-like compounds for MEF2 binding. This docking approach can be used to design and analyze new PAOA analogues with potentially greater affinity and selectivity. Some of the features of the structure are briefly described below to illustrate the principles to be used in designing new molecules that may bind MEF2 with higher affinity.

BML-210 adopts an extended conformation to bind into the hydrophobic pocket of MEF2 (FIG. 1). This is also the binding site for the MEF2-binding motif conserved in class IIa HDACs and Cabin1. Since one end of the electron density resembles a simple aromatic ring and is surrounded by a number of hydrophobic residues including Leu66, Leu67, Thr70, Leu66′, Leu67′ and Thr70′ (prime sign denote residues from the other monomer), we assigned this density to the phenyl group. The carbonyl group at this end is also in position to engage in hydrogen bonding interactions with Thr70′ (FIG. 1).

The structure-based design of new and optimized MEF2-binding small molecules can be achieved using several known structures of MEF2. We have now solved the crystal structures of three MEF2 complexes. Two of them contain a peptide derived from the MEF2-binding motif of Cabin1 and HDAC9, respectively (Guo et al., 2007; Han et al., 2005; Han et al., 2003), whereas the third one is the BML-210 complex described herein, which is the first structure showing how a small molecule can bind to MEF2. In all three complexes, the small molecule ligand, whether naturally occurring peptide or synthetic molecule, binds to the deep groove on the surface of MEF2 dimer (FIG. 1). Our previous studies show that Cabin1 and HDAC9 bind MEF2 through similar as well as distinct protein-protein interactions (FIG. 1) Interestingly, BML-210 seems to mimic some aspects of natural ligands in binding to MEF2. For example, the binding of the phenyl ring of PAOA to the central hydrophobic pocket formed by Leu66, Leu67, Thr70, Leu66′, Leu67′ and Thr70′ is reminiscent of that of Leu147 in HDAC9 (FIG. 1). Through detailed analyses of the three structures, we have identified a variety of structural features on the MEF2 groove that may be explored for small molecule binding, including a number of discrete hydrophobic pockets, hydrogen bond donors and acceptors, and several charged residues. We plan to utilize this structural information to design and optimize new series of small molecules that can bind selectively to MEF2.

Example 7 Structure-Guided Design of Small Molecule Inhibitors of the MEF2/HDAC Interaction

Using the crystal structures as guide, a large number of PAOA analogs that can provide the basis for identifying new MEF2-active small molecules was designed. The first group of analogs were designed to explore two general elements of the PAOA structure. First is the length and rigidity of the linker. Second are the functional groups and their positions on the two aromatic binding units. The electron density of the linker indicates that it adopts multiple conformations, suggesting non-optimal binding between PAOA and MEF2 in this region. In HDAC9, on the other hand, the aliphatic side chain of Lys144 and Val143 fill up the groove of MEF2 nicely to establish extensive Van der Waals contact and a hydrogen bond. Functional groups introduced at the PAOA linker to mimic/improve these natural interactions may enhance the binding affinity. The designed compounds were subjected to docking analysis mentioned above to filter out energetically unfavorable ones. The remaining molecules were synthesized using standard techniques and subjected to in vitro and in vivo analysis as described previously.

A first series of potential inhibitors (FIG. 2) was synthesized, and already found that different compounds showed significantly different activity in their ability to inhibit the reporter signal in the mammalian two-hybrid assay. Most interestingly, one of these, compound 4, showed similar activity as PAOA but with no effect on the control signal driven by GAL-VP-16, suggesting that this new derivative is more specific than PAOA. The ortho-aminoanilide moiety in PAOA has previously been postulated to be a zinc chelating group that can bind to the active site of class I and class II HDACs, but direct evidence for this mode of action is yet to be obtained. In compound 4, this Zinc chelating group is eliminated by moving the amino group to the meta position. Yet this derivative is as active as PAOA with less nonspecific effect, suggesting that the observed effect of PAOA inside cells, under our assay condition, is mainly due to its ability to disrupt MEF2:HDAC4 interaction rather than inhibiting the catalytic activity.

Example 8 Synthesis of Compound 10

The provided compounds can be prepared by adaptation of methods known in the art. For example, the synthesis of compound 10:

was prepared by the following steps:

-   Step 1: Pimelic acid (1 equiv) and 3-bromoaniline (1 equiv) were     added to flask and stirred at 130° C. overnight. The reaction     mixture was diluted in EtOAc and extracted with 10% potassium     hydroxide. The aqueous layer was acidified to pH˜2 with conc. HCl     and extracted with ethyl acetate. The organic layer was reduced     under vacuum and recrystallized with acetonitrile/water. -   Step 2. To a solution of phenylenediamine in dichloromethane was     added (Boc)₂O (1 equiv) at rt and the mixture was stirred overnight.     The reaction was concentrated under vacuum, diluted with ethyl     acetate, and was extracted with three times with water and brine.     The organic la yer was reduced under vacuum and recrystallized     chloroform/hexanes. -   Step 3. The product of Step 1 (100 mg) was dissolved in DMSO (3 mL)     and to this solution was added Hunig's base (1 equiv), HBTU (1     equiv), and the monoprotected phenylenediamine product of Step 2.     The resulting solution was stirred overnight at rt. The solution was     diluted with ethyl acetate and extracted with three times with     brine. The organic layer was reduced under vacuum and purified by     column chromatography (hexanes/ethyl acetate gradient). The isolated     product was dissolved in dichloromethane, cooled to ° C. and treated     with trifluoroacetic acid (1 mL). The solution was allowed to warm     to rt and stirred overnight. The reaction was neutralized with     sodium bicarbonate and concentrated under vacuum. The resulting     solid was dissolved in ethyl acetate and extracted with a saturated     sodium chloride solution. The organic layer was dried with magnesium     sulfate, filtered, concentrated under vacuum, and purified by column     chromatography (hexanes/ethyl acetate and dichloromethane/methanol     gradient). Evaporation of the solvents under vacuum, provided the     pure product 10, whose structure and purity was verified by NMR     spectroscopy.

Although the present invention has been described in terms of specific exemplary embodiments and examples, it will be appreciated that the embodiments disclosed herein are for illustrative purposes only and various modifications and alterations might be made by those skilled in the art without departing from the spirit and scope of the invention as set forth in the following claims.

TABLE 1 REMARK Date 2009-01-07 Time 10:43:15 PST -0800 (1231353795.26 s) REMARK PHENIX refinement REMARK REMARK ****************** INPUT FILES AND LABELS ****************************** REMARK Reflections: REMARK  file name: 3set-bm30-p1.mtz REMARK  labels: [′F_nat, SIGF_nat’] REMARK R-free flags: REMARK  file name: 3set-bm30-p1.mtz REMARK  label: FreeR_flag REMARK  test_flag_value: 0 REMARK Model file name(s): REMARK  /Users/rajadey/bml30/phenix/11.1_001_nr_h_001.pdb_modified.pdb REMARK REMARK ******************** REFINEMENT SUMMARY: QUICK FACTS ******************* REMARK Start: r_work = 0.2261 r_free = 0.2662 bonds = 0.010 angles = 1.585 REMARK Final: r_work = 0.2300 r_free = 0.2625 bonds = 0.004 angles = 0.999 REMARK ************************************************************************ REMARK REMARK ****************** REFINEMENT STATISTICS STEP BY STEP ****************** REMARK leading digit, like 1_, means number of macro-cycle REMARK 0: statistics at the very beginning when nothing is done yet REMARK 1_bss: bulk solvent correction and/or (anisotropic) scaling REMARK 1_xyz: refinement of coordinates REMARK 1_sar: simulated annealing refinement of x, y, z REMARK 1_gbr: group B-factor refinement REMARK ------------------------------------------------------------------------ REMARK  R-factors, x-ray target values and norm of gradient of x-ray target REMARK  stage r-work r-free xray_target_w xray_target_t REMARK   0: 0.3724 0.4597 4.600657e+00 4.693864e+00 REMARK   1_bss: 0.2261 0.2662 4.353757e+00 4.511409e+00 REMARK   1_sar: 0.2304 0.2635 4.369227e+00 4.510175e+00 REMARK   1_xyz: 0.2300 0.2624 4.366691e+00 4.507881e+00 REMARK   1_adp: 0.2313 0.2633 4.364563e+00 4.506710e+00 REMARK   1_bss: 0.2300 0.2625 4.363161e+00 4.505319e+00 REMARK ------------------------------------------------------------------------ REMARK  stage k_sol b_sol b11 b22 b33 b12 b13 b23 REMARK   0: 0.000 0.000 0.000 0.000 0.000 0.000 0.000 0.000 REMARK   1_bss: 0.364 20.242 −6.805 6.192 −3.021 −0.487 0.775 −11.187 REMARK   1_sar: 0.364 20.242 −6.805 6.192 −3.021 −0.487 0.775 −11.187 REMARK   1_xyz: 0.364 20.242 −6.805 6.192 −3.021 −0.487 0.775 −11.187 REMARK   1_adp: 0.364 20.242 −6.805 6.192 −3.021 −0.487 0.775 −11.187 REMARK   1_bss: 0.365 21.349 −5.565 7.438 −1.873 −0.502 0.768 −11.282 REMARK ------------------------------------------------------------------------ REMARK  stage <pher> fom alpha beta REMARK   0: 38.723 0.6722 0.4429 3605.155 REMARK   1_bss: 29.255 0.7800 0.4779 1636.075 REMARK   1_sar: 29.008 0.7829 0.4789 1613.168 REMARK   1_xyz: 29.000 0.7829 0.4786 1605.471 REMARK   1_adp: 28.879 0.7844 0.4600 1604.065 REMARK   1_bss: 28.857 0.7846 0.4744 1600.058 REMARK ------------------------------------------------------------------------ REMARK  stage angl bond chir dihe plan repu geom_target REMARK   0: 1.585 0.010 0.062 24.116 0.004 4.102 1.0603e−01 REMARK   1_bss: 1.585 0.010 0.062 24.116 0.004 4.102 1.0603e−01 REMARK   1_sar: 1.491 0.016 0.080 22.841 0.006 4.104 1.3573e−01 REMARK   1_xyz: 0.999 0.004 0.052 22.782 0.002 4.103 5.3401e−02 REMARK   1_adp: 0.999 0.004 0.052 22.782 0.002 4.103 5.3401e−02 REMARK   1_bss: 0.999 0.004 0.052 22.782 0.002 4.103 5.3401e−02 REMARK ------------------------------------------------------------------------ REMARK           Maximal deviations: REMARK  stage angl bond chir dihe plan repu |grad| REMARK   0: 19.277 0.072 0.199 87.514 0.017 2.477 7.1857e−02 REMARK   1_bss: 19.277 0.072 0.199 87.514 0.017 2.477 7.1857e−02 REMARK   1_sar: 13.759 0.149 0.349 82.939 0.024 2.483 2.0037e−01 REMARK   1_xyz: 5.840 0.026 0.193 83.107 0.009 2.480 2.2669e−02 REMARK   1_adp: 5.840 0.026 0.193 83.107 0.009 2.480 2.2669e−02 REMARK   1_bss: 5.840 0.026 0.193 83.107 0.009 2.480 2.2669e−02 REMARK ------------------------------------------------------------------------ REMARK  stage b_max b_min b_ave REMARK   0: 98.49 10.66 34.81 REMARK   1_bss: 98.49 10.66 34.81 REMARK   1_sar: 98.49 10.66 34.81 REMARK   1_xyz: 98.49 10.66 34.81 REMARK   1_adp: 97.61 8.23 33.04 REMARK   1_bss: 97.70 8.32 33.12 REMARK ------------------------------------------------------------------------ REMARK  stage Deviation of refined REMARK model from start model REMARK max min mean REMARK   0: 0.000 0.000 0.000 REMARK   1_bss: 0.000 0.000 0.000 REMARK   1_sar: 0.779 0.002 0.073 REMARK   1_xyz: 0.781 0.003 0.069 REMARK   1_adp: 0.781 0.003 0.069 REMARK   1_bss: 0.781 0.003 0.069 REMARK ------------------------------------------------------------------------ REMARK MODEL CONTENT. REMARK  ELEMENT ATOM RECORD COUNT OCCUPANCY SUM REMARK P 64 64.00 REMARK C 2188 2188.00 REMARK S 20 20.00 REMARK O 824 824.00 REMARK N 654 654.00 REMARK TOTAL 3750 3750.00 REMARK ------------------------------------------------------------------------ REMARK r_free_flags.md5.hexdigest c7ab61ecd5d91bd96f477e00cb52bbd9 REMARK REMARK IF THIS FILE IS FOR PDB DEPOSITION: REMOVE ALL FROM THIS LINE UP. REMARK 3 REMARK 3 REFINEMENT. REMARK 3  PROGRAM : PHENIX (phenix, refine) REMARK 3  AUTHORS : Paul Adams, Pavel Afonine, Vincent Chen, Ian REMARK 3 : Davis, Kreshna Gopal, Ralf Grosse-Kunstleve, REMARK 3 : Jeffrey Headd, Li-Wei Hung, Robert REMARK 3 : Immormino, Tom Ioerger, Airlie McCoy, Erik REMARK 3 : McKee, Nigel Moriarty, Reetal Pai, Randy REMARK 3 : Read, Jane Richardson, David Richardson, Tod REMARK 3 : Romo, Jim Sacchettini, Nicholas Sauter, REMARK 3 : Jacob Smith, Laurent Storoni, Tom REMARK 3 : Terwilliger, Peter Zwart REMARK 3 REMARK 3 REFINEMENT TARGET: ML REMARK 3 REMARK 3 DATA USED IN REFINEMENT. REMARK 3  RESOLUTION RANGE HIGH (ANGSTROMS): 2.434 REMARK 3  RESOLUTION RANGE LOW (ANGSTROMS): 33.444 REMARK 3  MIN(FOBS/SIGMA_FOBS): 2.00 REMARK 3  COMPLETENESS FOR RANGE (%): 94.76 REMARK 3  NUMBER OF REFLECTIONS: 19820 REMARK 3 REMARK 3 FIT TO DATA USED IN REFINEMENT. REMARK 3  R VALUE (WORKING + TEST SET): 0.2318 REMARK 3  R VALUE (WORKING SET): 0.2300 REMARK 3  FREE R VALUE: 0.2625 REMARK 3  FREE R VALUE TEST SET SIZE (%): 5.18 REMARK 3  FREE R VALUE TEST SET COUNT: 1026 REMARK 3 REMARK 3 FIT TO DATA USED IN REFINEMENT (IN BINS). REMARK 3  BIN RESOLUTION RANGE COMPL. NWORK NFREE RWORK RFREE REMARK 3 1 33.4475-4.6528 0.98 2734 158 0.1822 0.2100 REMARK 3 2 4.6528-3.6946 0.96 2695 176 0.1877 0.2158 REMARK 3 3 3.6946-3.2280 0.96 2707 127 0.2008 0.2520 REMARK 3 4 3.2280-2.9331 0.95 2707 141 0.2463 0.2810 REMARK 3 5 2.9331-2.7229 0.95 2703 142 0.2703 0.3447 REMARK 3 6 2.7229-2.5624 0.95 2664 142 0.2602 0.2953 REMARK 3 7 2.5624-2.4342 0.89 2584 140 0.2774 0.3272 REMARK 3 REMARK 3 BULK SOLVENT MODELLING. REMARK 3  METHOD USED: FLAT BULK SOLVENT MODEL REMARK 3  SOLVENT RADIUS: 1.11 REMARK 3  SHRINKAGE RADIUS: 0.90 REMARK 3  GRID STEP FACTOR: 4.00 REMARK 3  K_SOL: 0.365 REMARK 3  B_SOL: 21.349 REMARK 3 REMARK 3 ERROR ESTIMATES. REMARK 3  COORDINATE ERROR (MAXIMUM-LIKELIHOOD BASED): 0.40 REMARK 3  PHASE ERROR (DEGREES, MAXIMUM-LIKELIHOOD BASED): 28.86 REMARK 3 REMARK 3 OVERALL SCALE FACTORS. REMARK 3  SCALE = SUM(|F_OBS|*|F_MODEL|)/SUM(|F_MODEL|**2) : 0.5328 REMARK 3  ANISOTROPIC SCALE MATRIX ELEMENTS (IN CARTESIAN BASIS). REMARK 3  B11: −5.5649 REMARK 3  B22: 7.4379 REMARK 3  B33: −1.8730 REMARK 3  B12: −0.5019 REMARK 3  B13: 0.7684 REMARK 3  B23: −11.2823 REMARK 3 REMARK 3 R FACTOR FORMULA. REMARK 3  R = SUM(||F_OBS|−SCALE*|F_MODEL||)/SUM(|F_OBS|) REMARK 3 REMARK 3 TOTAL MODEL STRUCTURE FACTOR (F_MODEL). REMARK 3  F_MODEL = FB_CART * (F_CALC_ATOMS + F_BULK) REMARK 3  F_BULK = K_SOL * EXP(−B_SOL * S**2/4) * F_MASK REMARK 3  F_CALC_ATOMS = ATOMIC MODEL STRUCTURE FACTORS REMARK 3  FB_CART = EXP(−H(t) * A(−1) * B * A(−1t) * H) REMARK 3   A = orthogonalization matrix, H = MILLER INDEX REMARK 3   (t) = TRANSPOSE, (−1) = INVERSE REMARK 3 REMARK 3 STRUCTURE FACTORS CALCULATION ALGORITHM: FFT REMARK 3 REMARK 3 DEVIATIONS FROM IDEAL VALUES. REMARK 3 RMSD MAX COUNT REMARK 3  BOND: 0.004 0.026 3944 REMARK 3  ANGLE: 0.999 5.840 5574 REMARK 3  CHIRALITY: 0.052 0.193 630 REMARK 3  PLANARITY: 0.002 0.009 458 REMARK 3  DIHEDRAL: 22.782 83.107 1588 REMARK 3  MIN NONBONDED DISTANCE: 2.480 REMARK 3 REMARK 3 ATOMIC DISPLACEMENT PARAMETERS. REMARK 3  WILSON B: 32.79 REMARK 3  RMS(B_ISO_OR_EQUIVALENT_BONDED): 5.16 REMARK 3  ATOMS NUMBER OF ATOMS REMARK 3 ISO. ANISO. REMARK 3  ALL: 3750 0 REMARK 3  ALL (NO H): 3750 0 REMARK 3  SOLVENT: 0 0 REMARK 3  NON-SOLVENT: 3750 0 REMARK 3  HYDROGENS: 0 0 REMARK 3 CRYST1 41.567  61.622  61.478 114.12 89.99 89.95 P 1 SCALE1 0.024058 −0.000021 −0.000013 0.00000 SCALE2 0.000000 0.016228 0.007267 0.00000 SCALE3 0.000000 0.000000 0.017822 0.00000 ATOM 1 N GLY A 2 5.558 9.665 −0.148 1.00 40.48 A N ATOM 2 CA GLY A 2 6.598 10.216 0.701 1.00 40.72 A C ATOM 3 C GLY A 2 7.400 11.294 −0.003 1.00 44.33 A C ATOM 4 O GLY A 2 7.374 11.395 −1.230 1.00 46.18 A O ATOM 5 N ARG A 3 8.110 12.105 0.774 1.00 36.20 A N ATOM 6 CA ARG A 3 8.920 13.177 0.212 1.00 36.54 A C ATOM 7 C ARG A 3 9.915 12.608 −0.791 1.00 39.57 A C ATOM 8 O ARG A 3 10.208 13.222 −1.818 1.00 41.96 A O ATOM 9 CB ARG A 3 9.649 13.937 1.320 1.00 35.42 A C ATOM 10 CG ARG A 3 8.729 14.765 2.204 1.00 35.12 A C ATOM 11 CD ARG A 3 7.761 15.588 1.364 1.00 39.80 A C ATOM 12 NE ARG A 3 6.939 16.479 2.177 1.00 35.64 A N ATOM 13 CZ ARG A 3 7.340 17.668 2.620 1.00 40.68 A C ATOM 14 NH1 ARG A 3 8.558 18.111 2.336 1.00 32.06 A N ATOM 15 NH2 ARG A 3 6.522 18.412 3.353 1.00 37.63 A N ATOM 16 N LYS A 4 10.426 11.423 −0.481 1.00 34.29 A N ATOM 17 CA LYS A 4 11.319 10.710 −1.377 1.00 36.15 A C ATOM 18 C LYS A 4 10.906 9.247 −1.456 1.00 40.15 A C ATOM 19 O LYS A 4 10.372 8.689 −0.494 1.00 32.40 A O ATOM 20 CB LYS A 4 12.772 10.822 −0.901 1.00 37.35 A C ATOM 21 CG LYS A 4 13.368 12.214 −1.063 1.00 39.95 A C ATOM 22 CD LYS A 4 13.177 12.709 −2.489 1.00 40.70 A C ATOM 23 CE LYS A 4 13.272 14.224 −2.579 1.00 54.15 A C ATOM 24 NZ LYS A 4 12.727 14.727 −3.875 1.00 47.90 A N ATOM 25 N LYS A 5 11.141 8.633 −2.609 1.00 47.06 A N ATOM 26 CA LYS A 5 10.950 7.199 −2.740 1.00 44.41 A C ATOM 27 C LYS A 5 12.022 6.496 −1.927 1.00 46.84 A C ATOM 28 O LYS A 5 13.159 6.963 −1.860 1.00 51.80 A O ATOM 29 CB LYS A 5 11.037 6.767 −4.203 1.00 41.74 A C ATOM 30 CG LYS A 5 11.031 5.260 −4.387 1.00 49.22 A C ATOM 31 CD LYS A 5 10.524 4.863 −5.762 1.00 45.09 A C ATOM 32 CE LYS A 5 10.369 3.358 −5.865 1.00 49.10 A C ATOM 33 NZ LYS A 5 9.791 2.946 −7.171 1.00 54.49 A N ATOM 34 N ILE A 6 11.661 5.385 −1.296 1.00 40.65 A N ATOM 35 CA ILE A 6 12.634 4.589 −0.561 1.00 38.64 A C ATOM 36 C ILE A 6 12.794 3.198 −1.156 1.00 44.27 A C ATOM 37 O ILE A 6 11.989 2.759 −1.979 1.00 45.26 A O ATOM 38 CB ILE A 6 12.258 4.448 0.920 1.00 41.86 A C ATOM 39 CG1 ILE A 6 11.049 3.527 1.083 1.00 37.25 A C ATOM 40 CG2 ILE A 6 11.993 5.811 1.527 1.00 44.72 A C ATOM 41 CD1 ILE A 6 10.760 3.169 2.524 1.00 38.36 A C ATOM 42 N GLN A 7 13.848 2.512 −0.740 1.00 46.69 A N ATOM 43 CA GLN A 7 14.063 1.137 −1.149 1.00 45.95 A C ATOM 44 C GLN A 7 13.629 0.232 −0.017 1.00 44.14 A C ATOM 45 O GLN A 7 13.755 0.587 1.154 1.00 43.70 A O ATOM 46 CB GLN A 7 15.533 0.894 −1.493 1.00 54.70 A C ATOM 47 CG GLN A 7 15.980 1.567 −2.781 1.00 56.91 A C ATOM 48 CD GLN A 7 15.079 1.227 −3.957 1.00 73.33 A C ATOM 49 OE1 GLN A 7 14.583 0.104 −4.071 1.00 77.38 A O ATOM 50 NE2 GLN A 7 14.865 2.199 −4.840 1.00 72.72 A N ATOM 51 N ILE A 8 13.100 −0.933 −0.363 1.00 29.95 A N ATOM 52 CA ILE A 8 12.650 −1.870 0.650 1.00 22.66 A C ATOM 53 C ILE A 8 13.831 −2.654 1.210 1.00 25.91 A C ATOM 54 O ILE A 8 14.156 −3.748 0.749 1.00 26.66 A O ATOM 55 CB ILE A 8 11.550 −2.801 0.113 1.00 22.42 A C ATOM 56 CG1 ILE A 8 10.316 −1.972 −0.262 1.00 28.59 A C ATOM 57 CG2 ILE A 8 11.171 −3.841 1.145 1.00 19.64 A C ATOM 58 CD1 ILE A 8 9.862 −1.025 0.835 1.00 23.12 A C ATOM 59 N THR A 9 14.483 −2.072 2.208 1.00 25.29 A N ATOM 60 CA THR A 9 15.574 −2.752 2.889 1.00 25.71 A C ATOM 61 C THR A 9 15.621 −2.310 4.343 1.00 23.18 A C ATOM 62 O THR A 9 15.241 −1.185 4.669 1.00 26.78 A O ATOM 63 CB THR A 9 16.930 −2.491 2.204 1.00 29.73 A C ATOM 64 OG1 THR A 9 17.943 −3.307 2.811 1.00 36.44 A O ATOM 65 CG2 THR A 9 17.316 −1.019 2.312 1.00 22.13 A C ATOM 66 N ARG A 10 16.078 −3.209 5.209 1.00 22.93 A N ATOM 67 CA ARG A 10 16.159 −2.950 6.642 1.00 28.37 A C ATOM 68 C ARG A 10 16.693 −1.557 6.955 1.00 26.68 A C ATOM 69 O ARG A 10 17.735 −1.148 6.443 1.00 27.49 A O ATOM 70 CB ARG A 10 17.023 −4.007 7.327 1.00 26.07 A C ATOM 71 CG ARG A 10 16.937 −3.984 8.836 1.00 25.73 A C ATOM 72 CD ARG A 10 17.825 −5.050 9.458 1.00 26.43 A C ATOM 73 NE ARG A 10 17.850 −4.937 10.912 1.00 42.58 A N ATOM 74 CZ ARG A 10 18.617 −4.080 11.579 1.00 36.16 A C ATOM 75 NH1 ARG A 10 19.426 −3.263 10.917 1.00 40.67 A N ATOM 76 NH2 ARG A 10 18.578 −4.039 12.906 1.00 33.57 A N ATOM 77 N ILE A 11 15.952 −0.833 7.785 1.00 16.41 A N ATOM 78 CA ILE A 11 16.335 0.494 8.233 1.00 19.58 A C ATOM 79 C ILE A 11 17.336 0.359 9.378 1.00 23.29 A C ATOM 80 O ILE A 11 17.026 −0.225 10.420 1.00 24.17 A O ATOM 81 CB ILE A 11 15.093 1.288 8.695 1.00 24.31 A C ATOM 82 CG1 ILE A 11 14.176 1.563 7.502 1.00 17.73 A C ATOM 83 CG2 ILE A 11 15.493 2.592 9.378 1.00 17.50 A C ATOM 84 CD1 ILE A 11 12.849 2.159 7.874 1.00 19.62 A C ATOM 85 N MET A 12 18.540 0.887 9.176 1.00 25.66 A N ATOM 86 CA MET A 12 19.642 0.655 10.103 1.00 32.46 A C ATOM 87 C MET A 12 19.527 1.503 11.367 1.00 32.06 A C ATOM 88 O MET A 12 20.041 1.130 12.419 1.00 31.35 A O ATOM 89 CB MET A 12 20.989 0.904 9.414 1.00 27.61 A C ATOM 90 CG MET A 12 21.231 0.039 8.175 1.00 32.68 A C ATOM 91 SD MET A 12 21.173 −1.741 8.497 1.00 34.64 A S ATOM 92 CE MET A 12 22.666 −1.967 9.473 1.00 28.81 A C ATOM 93 N ASP A 13 18.851 2.643 11.249 1.00 53.42 A N ATOM 94 CA ASP A 13 18.670 3.570 12.363 1.00 55.93 A C ATOM 95 C ASP A 13 17.489 3.150 13.238 1.00 51.35 A C ATOM 96 O ASP A 13 16.336 3.215 12.809 1.00 49.36 A O ATOM 97 CB ASP A 13 18.460 4.991 11.826 1.00 56.02 A C ATOM 98 CG ASP A 13 17.848 5.929 12.857 1.00 72.21 A C ATOM 99 OD1 ASP A 13 18.235 5.856 14.043 1.00 78.94 A O ATOM 100 OD2 ASP A 13 16.982 6.749 12.477 1.00 67.36 A O ATOM 101 N GLU A 14 17.786 2.721 14.462 1.00 23.30 A N ATOM 102 CA GLU A 14 16.768 2.257 15.407 1.00 28.94 A C ATOM 103 C GLU A 14 15.663 3.287 15.636 1.00 34.28 A C ATOM 104 O GLU A 14 14.500 2.934 15.842 1.00 26.54 A O ATOM 105 CB GLU A 14 17.416 1.898 16.746 1.00 26.47 A C ATOM 106 CG GLU A 14 16.449 1.557 17.868 1.00 28.84 A C ATOM 107 CD GLU A 14 17.134 1.534 19.235 1.00 56.72 A C ATOM 108 OE1 GLU A 14 17.945 2.448 19.516 1.00 62.38 A O ATOM 109 OE2 GLU A 14 16.862 0.607 20.031 1.00 47.25 A O ATOM 110 N ARG A 15 16.028 4.562 15.600 1.00 47.85 A N ATOM 111 CA ARG A 15 15.056 5.624 15.804 1.00 40.56 A C ATOM 112 C ARG A 15 14.036 5.672 14.670 1.00 36.17 A C ATOM 113 O ARG A 15 12.834 5.592 14.914 1.00 32.41 A O ATOM 114 CB ARG A 15 15.755 6.974 15.963 1.00 49.45 A C ATOM 115 CG ARG A 15 14.860 8.051 16.537 1.00 54.99 A C ATOM 116 CD ARG A 15 15.619 8.954 17.492 1.00 65.98 A C ATOM 117 NE ARG A 15 14.821 9.226 18.684 1.00 72.44 A N ATOM 118 CZ ARG A 15 14.831 8.464 19.774 1.00 68.90 A C ATOM 119 NH1 ARG A 15 15.607 7.387 19.827 1.00 77.09 A N ATOM 120 NH2 ARG A 15 14.067 8.778 20.813 1.00 50.97 A N ATOM 121 N ASN A 16 14.511 5.798 13.433 1.00 34.37 A N ATOM 122 CA ASN A 16 13.610 5.821 12.282 1.00 30.83 A C ATOM 123 C ASN A 16 12.915 4.478 12.068 1.00 26.73 A C ATOM 124 O ASN A 16 11.836 4.417 11.485 1.00 25.88 A O ATOM 125 CB ASN A 16 14.340 6.245 11.000 1.00 36.12 A C ATOM 126 CG ASN A 16 13.409 6.283 9.777 1.00 44.40 A C ATOM 127 OD1 ASN A 16 12.378 6.962 9.784 1.00 34.71 A O ATOM 128 ND2 ASN A 16 13.776 5.552 8.725 1.00 30.96 A N ATOM 129 N ARG A 17 13.530 3.399 12.535 1.00 19.72 A N ATOM 130 CA ARG A 17 12.931 2.088 12.349 1.00 22.57 A C ATOM 131 C ARG A 17 11.716 1.960 13.253 1.00 23.83 A C ATOM 132 O ARG A 17 10.688 1.407 12.862 1.00 22.36 A O ATOM 133 CB ARG A 17 13.935 0.969 12.626 1.00 19.23 A C ATOM 134 CG ARG A 17 13.410 −0.412 12.279 1.00 19.82 A C ATOM 135 CD ARG A 17 14.508 −1.472 12.340 1.00 23.69 A C ATOM 136 NE ARG A 17 15.061 −1.590 13.683 1.00 27.46 A N ATOM 137 CZ ARG A 17 16.306 −1.263 14.017 1.00 30.61 A C ATOM 138 NH1 ARG A 17 17.159 −0.816 13.097 1.00 23.50 A N ATOM 139 NH2 ARG A 17 16.701 −1.399 15.276 1.00 31.20 A N ATOM 140 N GLN A 18 11.842 2.487 14.465 1.00 28.12 A N ATOM 141 CA GLN A 18 10.745 2.492 15.423 1.00 29.50 A C ATOM 142 C GLN A 18 9.583 3.356 14.921 1.00 25.82 A C ATOM 143 O GLN A 18 8.423 2.952 14.994 1.00 21.13 A O ATOM 144 CB GLN A 18 11.245 2.984 16.787 1.00 25.64 A C ATOM 145 CG GLN A 18 10.148 3.365 17.764 1.00 26.78 A C ATOM 146 CD GLN A 18 9.184 2.227 18.041 1.00 41.07 A C ATOM 147 OE1 GLN A 18 9.474 1.063 17.760 1.00 49.03 A O ATOM 148 NE2 GLN A 18 8.024 2.562 18.601 1.00 51.07 A N ATOM 149 N VAL A 19 9.910 4.541 14.410 1.00 27.77 A N ATOM 150 CA VAL A 19 8.916 5.456 13.861 1.00 26.66 A C ATOM 151 C VAL A 19 8.195 4.853 12.660 1.00 30.61 A C ATOM 152 O VAL A 19 6.964 4.827 12.610 1.00 30.39 A O ATOM 153 CB VAL A 19 9.561 6.781 13.424 1.00 29.19 A C ATOM 154 CG1 VAL A 19 8.619 7.558 12.511 1.00 27.30 A C ATOM 155 CG2 VAL A 19 9.944 7.606 14.640 1.00 27.00 A C ATOM 156 N THR A 20 8.965 4.376 11.689 1.00 24.75 A N ATOM 157 CA THR A 20 8.387 3.772 10.501 1.00 25.94 A C ATOM 158 C THR A 20 7.502 2.592 10.884 1.00 25.46 A C ATOM 159 O THR A 20 6.453 2.356 10.277 1.00 23.02 A O ATOM 160 CB THR A 20 9.473 3.280 9.537 1.00 28.24 A C ATOM 161 OG1 THR A 20 10.148 4.405 8.961 1.00 26.89 A O ATOM 162 CG2 THR A 20 8.850 2.434 8.430 1.00 23.49 A C ATOM 163 N PHE A 21 7.930 1.853 11.898 1.00 22.67 A N ATOM 164 CA PHE A 21 7.191 0.675 12.326 1.00 25.01 A C ATOM 165 C PHE A 21 5.824 1.033 12.904 1.00 23.93 A C ATOM 166 O PHE A 21 4.838 0.345 12.645 1.00 23.30 A O ATOM 167 CB PHE A 21 7.996 −0.136 13.339 1.00 20.65 A C ATOM 168 CG PHE A 21 7.201 −1.214 14.011 1.00 22.59 A C ATOM 169 CD1 PHE A 21 7.028 −2.448 13.400 1.00 17.85 A C ATOM 170 CD2 PHE A 21 6.616 −0.993 15.249 1.00 22.78 A C ATOM 171 CE1 PHE A 21 6.300 −3.446 14.014 1.00 20.66 A C ATOM 172 CE2 PHE A 21 5.876 −1.989 15.872 1.00 23.04 A C ATOM 173 CZ PHE A 21 5.720 −3.218 15.255 1.00 27.67 A C ATOM 174 N THR A 22 5.767 2.102 13.690 1.00 17.65 A N ATOM 175 CA THR A 22 4.503 2.537 14.271 1.00 18.23 A C ATOM 176 C THR A 22 3.548 3.066 13.196 1.00 16.79 A C ATOM 177 O THR A 22 2.354 2.772 13.221 1.00 17.70 A O ATOM 178 CB THR A 22 4.703 3.611 15.378 1.00 19.42 A C ATOM 179 OG1 THR A 22 5.340 3.023 16.521 1.00 16.50 A O ATOM 180 CG2 THR A 22 3.365 4.185 15.803 1.00 13.05 A C ATOM 181 N LYS A 23 4.070 3.850 12.258 1.00 21.15 A N ATOM 182 CA LYS A 23 3.245 4.375 11.177 1.00 22.13 A C ATOM 183 C LYS A 23 2.692 3.252 10.312 1.00 21.52 A C ATOM 184 O LYS A 23 1.487 3.165 10.100 1.00 22.00 A O ATOM 185 CB LYS A 23 4.032 5.350 10.300 1.00 25.46 A C ATOM 186 CG LYS A 23 4.247 6.727 10.908 1.00 31.78 A C ATOM 187 CD LYS A 23 5.175 7.556 10.019 1.00 35.00 A C ATOM 188 CE LYS A 23 5.361 8.963 10.558 1.00 38.42 A C ATOM 189 NZ LYS A 23 6.455 9.677 9.844 1.00 36.46 A N ATOM 190 N ARG A 24 3.578 2.393 9.818 1.00 18.04 A N ATOM 191 CA ARG A 24 3.181 1.335 8.887 1.00 17.50 A C ATOM 192 C ARG A 24 2.380 0.210 9.547 1.00 19.35 A C ATOM 193 O ARG A 24 1.571 −0.436 8.878 1.00 18.00 A O ATOM 194 CB ARG A 24 4.395 0.765 8.149 1.00 14.94 A C ATOM 195 CG ARG A 24 4.892 1.624 6.987 1.00 16.36 A C ATOM 196 CD ARG A 24 6.120 0.999 6.313 1.00 15.51 A C ATOM 197 NE ARG A 24 6.453 1.675 5.062 1.00 17.77 A N ATOM 198 CZ ARG A 24 6.091 1.244 3.855 1.00 19.55 A C ATOM 199 NH1 ARG A 24 5.388 0.122 3.722 1.00 19.36 A N ATOM 200 NH2 ARG A 24 6.430 1.934 2.778 1.00 14.87 A N ATOM 201 N LYS A 25 2.600 −0.029 10.843 1.00 19.64 A N ATOM 202 CA LYS A 25 1.820 −1.041 11.560 1.00 20.34 A C ATOM 203 C LYS A 25 0.370 −0.608 11.601 1.00 20.24 A C ATOM 204 O LYS A 25 −0.537 −1.397 11.351 1.00 20.44 A O ATOM 205 CB LYS A 25 2.326 −1.257 12.987 1.00 26.21 A C ATOM 206 CG LYS A 25 1.347 −2.046 13.867 1.00 22.43 A C ATOM 207 CD LYS A 25 2.031 −2.639 15.101 1.00 28.10 A C ATOM 208 CE LYS A 25 2.524 −1.564 16.083 1.00 24.12 A C ATOM 209 NZ LYS A 25 1.411 −0.839 16.761 1.00 21.37 A N ATOM 210 N PHE A 26 0.160 0.661 11.917 1.00 16.23 A N ATOM 211 CA PHE A 26 −1.165 1.248 11.835 1.00 18.62 A C ATOM 212 C PHE A 26 −1.732 1.076 10.415 1.00 18.38 A C ATOM 213 O PHE A 26 −2.837 0.573 10.234 1.00 19.75 A O ATOM 214 CB PHE A 26 −1.101 2.727 12.213 1.00 15.46 A C ATOM 215 CG PHE A 26 −2.443 3.384 12.314 1.00 19.64 A C ATOM 216 CD1 PHE A 26 −3.053 3.558 13.548 1.00 22.13 A C ATOM 217 CD2 PHE A 26 −3.095 3.834 11.177 1.00 17.94 A C ATOM 218 CE1 PHE A 26 −4.290 4.168 13.645 1.00 23.01 A C ATOM 219 CE2 PHE A 26 −4.329 4.440 11.266 1.00 21.01 A C ATOM 220 CZ PHE A 26 −4.929 4.609 12.505 1.00 27.60 A C ATOM 221 N GLY A 27 −0.962 1.487 9.413 1.00 27.12 A N ATOM 222 CA GLY A 27 −1.369 1.366 8.024 1.00 25.34 A C ATOM 223 C GLY A 27 −1.735 −0.049 7.618 1.00 23.53 A C ATOM 224 O GLY A 27 −2.658 −0.250 6.832 1.00 25.30 A O ATOM 225 N LEU A 28 −1.017 −1.032 8.154 1.00 20.30 A N ATOM 226 CA LEU A 28 −1.255 −2.431 7.800 1.00 20.79 A C ATOM 227 C LEU A 28 −2.542 −2.957 8.432 1.00 19.85 A C ATOM 228 O LEU A 28 −3.313 −3.672 7.790 1.00 17.99 A O ATOM 229 CB LEU A 28 −0.070 −3.310 8.210 1.00 23.59 A C ATOM 230 CG LEU A 28 −0.132 −4.788 7.794 1.00 20.17 A C ATOM 231 CD1 LEU A 28 −0.146 −4.926 6.293 1.00 16.98 A C ATOM 232 CD2 LEU A 28 1.026 −5.582 8.385 1.00 17.88 A C ATOM 233 N MET A 29 −2.774 −2.585 9.690 1.00 23.01 A N ATOM 234 CA MET A 29 −3.980 −3.002 10.395 1.00 20.12 A C ATOM 235 C MET A 29 −5.208 −2.346 9.777 1.00 18.22 A C ATOM 236 O MET A 29 −6.250 −2.976 9.629 1.00 16.78 A O ATOM 237 CB MET A 29 −3.889 −2.672 11.887 1.00 20.50 A C ATOM 238 CG MET A 29 −2.792 −3.423 12.641 1.00 20.16 A C ATOM 239 SD MET A 29 −3.158 −3.552 14.417 1.00 22.93 A S ATOM 240 CE MET A 29 −1.718 −4.473 14.963 1.00 25.26 A C ATOM 241 N LYS A 30 −5.082 −1.079 9.406 1.00 21.44 A N ATOM 242 CA LYS A 30 −6.195 −0.385 8.770 1.00 22.10 A C ATOM 243 C LYS A 30 −6.676 −1.145 7.529 1.00 21.81 A C ATOM 244 O LYS A 30 −7.861 −1.459 7.403 1.00 24.17 A O ATOM 245 CB LYS A 30 −5.813 1.053 8.416 1.00 20.87 A C ATOM 246 CG LYS A 30 −6.980 1.885 7.914 1.00 29.30 A C ATOM 247 CD LYS A 30 −6.576 3.329 7.647 1.00 29.06 A C ATOM 248 CE LYS A 30 −7.756 4.132 7.118 1.00 35.72 A C ATOM 249 NZ LYS A 30 −7.340 5.436 6.528 1.00 30.83 A N ATOM 250 N LYS A 31 −5.756 −1.460 6.623 1.00 18.84 A N ATOM 251 CA LYS A 31 −6.119 −2.177 5.399 1.00 22.05 A C ATOM 252 C LYS A 31 −6.644 −3.592 5.653 1.00 17.61 A C ATOM 253 O LYS A 31 −7.568 −4.043 4.985 1.00 21.05 A O ATOM 254 CB LYS A 31 −4.951 −2.188 4.412 1.00 18.86 A C ATOM 255 CG LYS A 31 −4.954 −0.991 3.476 1.00 20.01 A C ATOM 256 CD LYS A 31 −3.568 −0.685 2.946 1.00 22.22 A C ATOM 257 CE LYS A 31 −3.641 0.064 1.623 1.00 21.55 A C ATOM 258 NZ LYS A 31 −4.901 0.856 1.487 1.00 21.23 A N ATOM 259 N ALA A 32 −6.069 −4.283 6.630 1.00 13.45 A N ATOM 260 CA ALA A 32 −6.528 −5.624 6.967 1.00 13.40 A C ATOM 261 C ALA A 32 −7.983 −5.576 7.417 1.00 17.70 A C ATOM 262 O ALA A 32 −8.813 −6.346 6.928 1.00 17.45 A O ATOM 263 CB ALA A 32 −5.645 −6.244 8.043 1.00 12.68 A C ATOM 264 N TYR A 33 −8.285 −4.664 8.343 1.00 22.08 A N ATOM 265 CA TYR A 33 −9.655 −4.417 8.791 1.00 21.79 A C ATOM 266 C TYR A 33 −10.596 −4.066 7.633 1.00 24.76 A C ATOM 267 O TYR A 33 −11.714 −4.577 7.554 1.00 25.28 A O ATOM 268 CB TYR A 33 −9.682 −3.303 9.848 1.00 26.33 A C ATOM 269 CG TYR A 33 −11.001 −2.557 9.934 1.00 24.65 A C ATOM 270 CD1 TYR A 33 −12.060 −3.060 10.676 1.00 28.98 A C ATOM 271 CD2 TYR A 33 −11.184 −1.349 9.271 1.00 26.32 A C ATOM 272 CE1 TYR A 33 −13.266 −2.382 10.757 1.00 30.58 A C ATOM 273 CE2 TYR A 33 −12.389 −0.664 9.341 1.00 25.98 A C ATOM 274 CZ TYR A 33 −13.424 −1.185 10.087 1.00 31.84 A C ATOM 275 OH TYR A 33 −14.621 −0.509 10.165 1.00 30.84 A O ATOM 276 N GLU A 34 −10.146 −3.187 6.744 1.00 23.16 A N ATOM 277 CA GLU A 34 −10.947 −2.799 5.589 1.00 21.92 A C ATOM 278 C GLU A 34 −11.227 −3.986 4.675 1.00 22.46 A C ATOM 279 O GLU A 34 −12.328 −4.113 4.129 1.00 22.16 A O ATOM 280 CB GLU A 34 −10.266 −1.673 4.810 1.00 21.12 A C ATOM 281 CG GLU A 34 −10.229 −0.344 5.557 1.00 20.36 A C ATOM 282 CD GLU A 34 −9.648 0.778 4.718 1.00 21.90 A C ATOM 283 OE1 GLU A 34 −9.002 0.483 3.690 1.00 23.00 A O ATOM 284 OE2 GLU A 34 −9.836 1.956 5.081 1.00 19.62 A O ATOM 285 N LEU A 35 −10.244 −4.867 4.520 1.00 19.11 A N ATOM 286 CA LEU A 35 −10.450 −6.059 3.696 1.00 19.55 A C ATOM 287 C LEU A 35 −11.446 −7.026 4.342 1.00 20.70 A C ATOM 288 O LEU A 35 −12.263 −7.643 3.652 1.00 22.13 A O ATOM 289 CB LEU A 35 −9.129 −6.769 3.392 1.00 16.66 A C ATOM 290 CG LEU A 35 −9.271 −8.010 2.511 1.00 19.14 A C ATOM 291 CD1 LEU A 35 −9.903 −7.645 1.173 1.00 17.50 A C ATOM 292 CD2 LEU A 35 −7.933 −8.701 2.306 1.00 18.21 A C ATOM 293 N SER A 36 −11.379 −7.157 5.662 1.00 22.42 A N ATOM 294 CA SER A 36 −12.327 −8.001 6.379 1.00 27.64 A C ATOM 295 C SER A 36 −13.764 −7.538 6.134 1.00 24.59 A C ATOM 296 O SER A 36 −14.650 −8.346 5.866 1.00 26.35 A O ATOM 297 CB SER A 36 −12.026 −8.000 7.879 1.00 29.01 A C ATOM 298 OG SER A 36 −12.983 −8.771 8.588 1.00 28.51 A O ATOM 299 N VAL A 37 −13.983 −6.230 6.217 1.00 20.31 A N ATOM 300 CA VAL A 37 −15.321 −5.664 6.084 1.00 19.68 A C ATOM 301 C VAL A 37 −15.815 −5.656 4.637 1.00 21.49 A C ATOM 302 O VAL A 37 −16.905 −6.141 4.344 1.00 21.28 A O ATOM 303 CB VAL A 37 −15.382 −4.229 6.643 1.00 20.47 A C ATOM 304 CG1 VAL A 37 −16.750 −3.610 6.387 1.00 17.32 A C ATOM 305 CG2 VAL A 37 −15.060 −4.228 8.124 1.00 21.67 A C ATOM 306 N LEU A 38 −15.016 −5.093 3.738 1.00 24.67 A N ATOM 307 CA LEU A 38 −15.401 −4.971 2.338 1.00 20.97 A C ATOM 308 C LEU A 38 −15.745 −6.319 1.717 1.00 22.62 A C ATOM 309 O LEU A 38 −16.724 −6.438 0.975 1.00 24.77 A O ATOM 310 CB LEU A 38 −14.274 −4.327 1.527 1.00 20.39 A C ATOM 311 CG LEU A 38 −13.936 −2.859 1.771 1.00 18.81 A C ATOM 312 CD1 LEU A 38 −12.570 −2.532 1.177 1.00 16.96 A C ATOM 313 CD2 LEU A 38 −15.017 −1.951 1.204 1.00 19.42 A C ATOM 314 N CYS A 39 −14.937 −7.331 2.013 1.00 21.00 A N ATOM 315 CA CYS A 39 −15.071 −8.615 1.330 1.00 22.90 A C ATOM 316 C CYS A 39 −15.531 −9.750 2.239 1.00 24.81 A C ATOM 317 O CYS A 39 −15.504 −10.915 1.847 1.00 28.63 A O ATOM 318 CB CYS A 39 −13.757 −8.989 0.640 1.00 18.48 A C ATOM 319 SG CYS A 39 −13.163 −7.706 −0.472 1.00 18.20 A S ATOM 320 N ASP A 40 −15.944 −9.413 3.455 1.00 28.63 A N ATOM 321 CA ASP A 40 −16.503 −10.417 4.351 1.00 30.28 A C ATOM 322 C ASP A 40 −15.583 −11.631 4.483 1.00 31.00 A C ATOM 323 O ASP A 40 −15.878 −12.695 3.944 1.00 30.22 A O ATOM 324 CB ASP A 40 −17.876 −10.858 3.831 1.00 27.25 A C ATOM 325 CG ASP A 40 −18.585 −11.821 4.770 1.00 31.14 A C ATOM 326 OD1 ASP A 40 −18.189 −11.932 5.948 1.00 32.84 A O ATOM 327 OD2 ASP A 40 −19.552 −12.472 4.318 1.00 47.25 A O ATOM 328 N CYS A 41 −14.469 −11.472 5.192 1.00 28.67 A N ATOM 329 CA CYS A 41 −13.600 −12.611 5.476 1.00 34.11 A C ATOM 330 C CYS A 41 −12.962 −12.566 6.867 1.00 33.64 A C ATOM 331 O CYS A 41 −12.839 −11.500 7.470 1.00 32.01 A O ATOM 332 CB CYS A 41 −12.530 −12.771 4.390 1.00 34.49 A C ATOM 333 SG CYS A 41 −11.901 −11.242 3.695 1.00 42.38 A S ATOM 334 N GLU A 42 −12.589 −13.739 7.377 1.00 35.13 A N ATOM 335 CA GLU A 42 −11.835 −13.837 8.617 1.00 31.41 A C ATOM 336 C GLU A 42 −10.393 −13.499 8.312 1.00 31.12 A C ATOM 337 O GLU A 42 −9.852 −13.934 7.299 1.00 34.59 A O ATOM 338 CB GLU A 42 −11.864 −15.258 9.177 1.00 36.09 A C ATOM 339 CG GLU A 42 −13.223 −15.801 9.546 1.00 50.30 A C ATOM 340 CD GLU A 42 −13.107 −17.105 10.310 1.00 48.91 A C ATOM 341 OE1 GLU A 42 −13.992 −17.973 10.160 1.00 69.71 A O ATOM 342 OE2 GLU A 42 −12.118 −17.264 11.053 1.00 39.96 A O ATOM 343 N ILE A 43 −9.760 −12.740 9.196 1.00 22.52 A N ATOM 344 CA ILE A 43 −8.359 −12.401 9.012 1.00 18.82 A C ATOM 345 C ILE A 43 −7.604 −12.413 10.333 1.00 18.26 A C ATOM 346 O ILE A 43 −8.152 −12.074 11.378 1.00 19.33 A O ATOM 347 CB ILE A 43 −8.204 −11.046 8.308 1.00 18.81 A C ATOM 348 CG1 ILE A 43 −8.579 −11.199 6.828 1.00 19.26 A C ATOM 349 CG2 ILE A 43 −6.774 −10.523 8.471 1.00 14.71 A C ATOM 350 CD1 ILE A 43 −8.902 −9.910 6.115 1.00 17.63 A C ATOM 351 N ALA A 44 −6.347 −12.832 10.282 1.00 20.70 A N ATOM 352 CA ALA A 44 −5.490 −12.809 11.456 1.00 22.51 A C ATOM 353 C ALA A 44 −4.138 −12.232 11.077 1.00 21.54 A C ATOM 354 O ALA A 44 −3.557 −12.601 10.061 1.00 24.49 A O ATOM 355 CB ALA A 44 −5.335 −14.210 12.044 1.00 20.18 A C ATOM 356 N LEU A 45 −3.645 −11.321 11.902 1.00 17.20 A N ATOM 357 CA LEU A 45 −2.373 −10.673 11.656 1.00 15.17 A C ATOM 358 C LEU A 45 −1.574 −10.679 12.949 1.00 18.70 A C ATOM 359 O LEU A 45 −1.992 −10.088 13.944 1.00 18.56 A O ATOM 360 CB LEU A 45 −2.605 −9.233 11.184 1.00 17.70 A C ATOM 361 CG LEU A 45 −1.376 −8.343 10.969 1.00 18.97 A C ATOM 362 CD1 LEU A 45 −0.350 −9.045 10.095 1.00 13.61 A C ATOM 363 CD2 LEU A 45 −1.769 −6.995 10.371 1.00 15.25 A C ATOM 364 N ILE A 46 −0.435 −11.361 12.938 1.00 26.22 A N ATOM 365 CA ILE A 46 0.447 −11.399 14.100 1.00 28.53 A C ATOM 366 C ILE A 46 1.785 −10.754 13.769 1.00 28.91 A C ATOM 367 O ILE A 46 2.450 −11.141 12.804 1.00 26.44 A O ATOM 368 CB ILE A 46 0.683 −12.842 14.585 1.00 31.11 A C ATOM 369 CG1 ILE A 46 −0.604 −13.416 15.186 1.00 29.74 A C ATOM 370 CG2 ILE A 46 1.810 −12.883 15.600 1.00 27.36 A C ATOM 371 CD1 ILE A 46 −0.564 −14.908 15.418 1.00 29.20 A C ATOM 372 N ILE A 47 2.179 −9.771 14.572 1.00 23.77 A N ATOM 373 CA ILE A 47 3.412 −9.032 14.328 1.00 24.05 A C ATOM 374 C ILE A 47 4.284 −8.942 15.572 1.00 24.16 A C ATOM 375 O ILE A 47 3.843 −8.444 16.608 1.00 27.34 A O ATOM 376 CB ILE A 47 3.118 −7.585 13.884 1.00 24.61 A C ATOM 377 CG1 ILE A 47 2.161 −7.561 12.691 1.00 22.79 A C ATOM 378 CG2 ILE A 47 4.420 −6.847 13.569 1.00 25.34 A C ATOM 379 CD1 ILE A 47 1.725 −6.168 12.318 1.00 20.83 A C ATOM 380 N PHE A 48 5.521 −9.410 15.467 1.00 22.85 A N ATOM 381 CA PHE A 48 6.512 −9.211 16.518 1.00 22.42 A C ATOM 382 C PHE A 48 7.548 −8.240 15.990 1.00 25.30 A C ATOM 383 O PHE A 48 8.218 −8.543 15.007 1.00 29.18 A O ATOM 384 CB PHE A 48 7.226 −10.522 16.859 1.00 25.20 A C ATOM 385 CG PHE A 48 6.317 −11.609 17.348 1.00 23.66 A C ATOM 386 CD1 PHE A 48 5.817 −12.556 16.471 1.00 22.65 A C ATOM 387 CD2 PHE A 48 5.979 −11.699 18.688 1.00 27.45 A C ATOM 388 CE1 PHE A 48 4.982 −13.567 16.920 1.00 23.46 A C ATOM 389 CE2 PHE A 48 5.147 −12.709 19.142 1.00 29.13 A C ATOM 390 CZ PHE A 48 4.649 −13.645 18.251 1.00 24.78 A C ATOM 391 N ASN A 49 7.701 −7.086 16.631 1.00 25.18 A N ATOM 392 CA ASN A 49 8.713 −6.132 16.184 1.00 24.60 A C ATOM 393 C ASN A 49 10.116 −6.668 16.455 1.00 25.56 A C ATOM 394 O ASN A 49 10.268 −7.771 16.984 1.00 25.60 A O ATOM 395 CB ASN A 49 8.504 −4.745 16.807 1.00 22.23 A C ATOM 396 CG ASN A 49 8.835 −4.702 18.290 1.00 28.49 A C ATOM 397 OD1 ASN A 49 9.250 −5.702 18.884 1.00 28.05 A O ATOM 398 ND2 ASN A 49 8.654 −3.532 18.895 1.00 25.55 A N ATOM 399 N SER A 50 11.135 −5.899 16.081 1.00 25.43 A N ATOM 400 CA SER A 50 12.519 −6.333 16.254 1.00 31.36 A C ATOM 401 C SER A 50 12.881 −6.563 17.719 1.00 35.94 A C ATOM 402 O SER A 50 13.703 −7.423 18.026 1.00 40.93 A O ATOM 403 CB SER A 50 13.492 −5.338 15.610 1.00 31.21 A C ATOM 404 OG SER A 50 13.188 −4.003 15.972 1.00 36.34 A O ATOM 405 N SER A 51 12.263 −5.801 18.618 1.00 40.78 A N ATOM 406 CA SER A 51 12.503 −5.959 20.055 1.00 40.97 A C ATOM 407 C SER A 51 11.650 −7.080 20.648 1.00 44.26 A C ATOM 408 O SER A 51 11.588 −7.245 21.867 1.00 37.55 A O ATOM 409 CB SER A 51 12.231 −4.650 20.801 1.00 35.21 A C ATOM 410 OG SER A 51 12.982 −3.582 20.252 1.00 42.54 A O ATOM 411 N ASN A 52 10.978 −7.827 19.775 1.00 42.32 A N ATOM 412 CA ASN A 52 10.240 −9.032 20.156 1.00 39.65 A C ATOM 413 C ASN A 52 8.901 −8.797 20.870 1.00 39.57 A C ATOM 414 O ASN A 52 8.307 −9.735 21.406 1.00 40.20 A O ATOM 415 CB ASN A 52 11.123 −9.962 20.990 1.00 40.53 A C ATOM 416 CG ASN A 52 11.150 −11.379 20.449 1.00 54.19 A C ATOM 417 OD1 ASN A 52 11.503 −11.606 19.288 1.00 47.98 A O ATOM 418 ND2 ASN A 52 10.787 −12.343 21.290 1.00 54.16 A N ATOM 419 N LYS A 53 8.420 −7.558 20.880 1.00 28.18 A N ATOM 420 CA LYS A 53 7.092 −7.297 21.431 1.00 31.87 A C ATOM 421 C LYS A 53 5.992 −7.674 20.436 1.00 29.62 A C ATOM 422 O LYS A 53 6.091 −7.392 19.242 1.00 24.49 A O ATOM 423 CB LYS A 53 6.927 −5.841 21.878 1.00 29.10 A C ATOM 424 CG LYS A 53 5.561 −5.579 22.522 1.00 36.89 A C ATOM 425 CD LYS A 53 5.352 −4.114 22.898 1.00 32.62 A C ATOM 426 CE LYS A 53 3.962 −3.900 23.489 1.00 35.52 A C ATOM 427 NZ LYS A 53 3.638 −2.459 23.700 1.00 34.56 A N ATOM 428 N LEU A 54 4.941 −8.303 20.951 1.00 30.84 A N ATOM 429 CA LEU A 54 3.848 −8.811 20.135 1.00 25.96 A C ATOM 430 C LEU A 54 2.779 −7.753 19.832 1.00 24.55 A C ATOM 431 O LEU A 54 2.358 −7.010 20.711 1.00 32.55 A O ATOM 432 CB LEU A 54 3.212 −10.008 20.844 1.00 30.00 A C ATOM 433 CG LEU A 54 1.897 −10.574 20.308 1.00 33.18 A C ATOM 434 CD1 LEU A 54 2.067 −11.111 18.891 1.00 23.66 A C ATOM 435 CD2 LEU A 54 1.372 −11.655 21.245 1.00 28.80 A C ATOM 436 N PHE A 55 2.358 −7.687 18.574 1.00 25.64 A N ATOM 437 CA PHE A 55 1.218 −6.867 18.175 1.00 25.15 A C ATOM 438 C PHE A 55 0.298 −7.729 17.324 1.00 23.57 A C ATOM 439 O PHE A 55 0.767 −8.560 16.554 1.00 29.95 A O ATOM 440 CB PHE A 55 1.673 −5.645 17.378 1.00 25.44 A C ATOM 441 CG PHE A 55 2.542 −4.702 18.157 1.00 20.82 A C ATOM 442 CD1 PHE A 55 3.918 −4.851 18.163 1.00 23.48 A C ATOM 443 CD2 PHE A 55 1.980 −3.663 18.880 1.00 24.05 A C ATOM 444 CE1 PHE A 55 4.723 −3.984 18.881 1.00 28.55 A C ATOM 445 CE2 PHE A 55 2.776 −2.786 19.602 1.00 27.58 A C ATOM 446 CZ PHE A 55 4.152 −2.945 19.601 1.00 31.46 A C ATOM 447 N GLN A 56 −1.008 −7.542 17.456 1.00 24.49 A N ATOM 448 CA GLN A 56 −1.934 −8.428 16.774 1.00 25.21 A C ATOM 449 C GLN A 56 −3.247 −7.778 16.369 1.00 27.21 A C ATOM 450 O GLN A 56 −3.723 −6.842 17.009 1.00 29.58 A O ATOM 451 CB GLN A 56 −2.216 −9.658 17.641 1.00 31.95 A C ATOM 452 CG GLN A 56 −2.730 −9.336 19.035 1.00 28.95 A C ATOM 453 CD GLN A 56 −2.850 −10.574 19.914 1.00 40.70 A C ATOM 454 OE1 GLN A 56 −3.506 −11.554 19.547 1.00 35.84 A O ATOM 455 NE2 GLN A 56 −2.216 −10.532 21.084 1.00 38.27 A N ATOM 456 N TYR A 57 −3.819 −8.294 15.287 1.00 24.23 A N ATOM 457 CA TYR A 57 −5.164 −7.950 14.866 1.00 23.97 A C ATOM 458 C TYR A 57 −5.876 −9.216 14.415 1.00 25.38 A C ATOM 459 O TYR A 57 −5.253 −10.121 13.855 1.00 29.08 A O ATOM 460 CB TYR A 57 −5.164 −6.947 13.708 1.00 28.41 A C ATOM 461 CG TYR A 57 −6.492 −6.947 12.975 1.00 26.05 A C ATOM 462 CD1 TYR A 57 −7.586 −6.260 13.483 1.00 25.02 A C ATOM 463 CD2 TYR A 57 −6.665 −7.675 11.806 1.00 22.16 A C ATOM 464 CE1 TYR A 57 −8.809 −6.279 12.836 1.00 23.65 A C ATOM 465 CE2 TYR A 57 −7.883 −7.699 11.150 1.00 21.67 A C ATOM 466 CZ TYR A 57 −8.952 −7.002 11.669 1.00 25.56 A C ATOM 467 OH TYR A 57 −10.168 −7.017 11.021 1.00 25.78 A O ATOM 468 N ALA A 58 −7.183 −9.270 14.645 1.00 13.45 A N ATOM 469 CA ALA A 58 −8.001 −10.369 14.156 1.00 18.60 A C ATOM 470 C ALA A 58 −9.446 −9.907 13.982 1.00 17.25 A C ATOM 471 O ALA A 58 −9.962 −9.165 14.810 1.00 18.31 A O ATOM 472 CB ALA A 58 −7.918 −11.548 15.100 1.00 19.29 A C ATOM 473 N SER A 59 −10.092 −10.341 12.902 1.00 19.89 A N ATOM 474 CA SER A 59 −11.471 −9.942 12.632 1.00 23.73 A C ATOM 475 C SER A 59 −12.451 −10.641 13.572 1.00 25.80 A C ATOM 476 O SER A 59 −13.630 −10.306 13.605 1.00 26.75 A O ATOM 477 CB SER A 59 −11.849 −10.200 11.170 1.00 21.23 A C ATOM 478 OG SER A 59 −11.812 −11.582 10.859 1.00 20.25 A O ATOM 479 N THR A 60 −11.952 −11.625 14.318 1.00 40.12 A N ATOM 480 CA THR A 60 −12.699 −12.265 15.398 1.00 40.61 A C ATOM 481 C THR A 60 −11.684 −12.718 16.431 1.00 43.22 A C ATOM 482 O THR A 60 −10.506 −12.388 16.322 1.00 43.35 A O ATOM 483 CB THR A 60 −13.469 −13.508 14.926 1.00 49.84 A C ATOM 484 OG1 THR A 60 −12.545 −14.580 14.689 1.00 54.22 A O ATOM 485 CG2 THR A 60 −14.257 −13.220 13.655 1.00 57.35 A C ATOM 486 N ASP A 61 −12.126 −13.481 17.426 1.00 31.10 A N ATOM 487 CA ASP A 61 −11.191 −14.035 18.405 1.00 35.26 A C ATOM 488 C ASP A 61 −10.038 −14.736 17.691 1.00 35.75 A C ATOM 489 O ASP A 61 −10.254 −15.609 16.839 1.00 32.83 A O ATOM 490 CB ASP A 61 −11.891 −15.008 19.363 1.00 37.37 A C ATOM 491 CG ASP A 61 −12.676 −14.296 20.454 1.00 40.45 A C ATOM 492 OD1 ASP A 61 −13.084 −13.137 20.237 1.00 42.00 A O ATOM 493 OD2 ASP A 61 −12.883 −14.895 21.530 1.00 47.45 A O ATOM 494 N MET A 62 −8.817 −14.343 18.038 1.00 45.71 A N ATOM 495 CA MET A 62 −7.619 −14.912 17.430 1.00 39.27 A C ATOM 496 C MET A 62 −7.597 −16.434 17.508 1.00 42.49 A C ATOM 497 O MET A 62 −7.261 −17.105 16.534 1.00 45.64 A O ATOM 498 CB MET A 62 −6.363 −14.350 18.092 1.00 31.62 A C ATOM 499 CG MET A 62 −5.077 −14.872 17.479 1.00 41.13 A C ATOM 500 SD MET A 62 −4.955 −14.470 15.724 1.00 33.45 A S ATOM 501 CE MET A 62 −4.563 −12.724 15.799 1.00 30.51 A C ATOM 502 N ASP A 63 −7.956 −16.971 18.670 1.00 50.73 A N ATOM 503 CA ASP A 63 −7.911 −18.411 18.898 1.00 51.32 A C ATOM 504 C ASP A 63 −8.782 −19.163 17.898 1.00 45.54 A C ATOM 505 O ASP A 63 −8.557 −20.342 17.631 1.00 52.73 A O ATOM 506 CB ASP A 63 −8.338 −18.744 20.334 1.00 56.83 A C ATOM 507 CG ASP A 63 −9.849 −18.803 20.499 1.00 68.01 A C ATOM 508 OD1 ASP A 63 −10.443 −19.866 20.207 1.00 61.02 A O ATOM 509 OD2 ASP A 63 −10.442 −17.792 20.934 1.00 68.32 A O ATOM 510 N LYS A 64 −9.775 −18.478 17.344 1.00 35.97 A N ATOM 511 CA LYS A 64 −10.681 −19.107 16.389 1.00 37.94 A C ATOM 512 C LYS A 64 −10.058 −19.207 14.997 1.00 40.31 A C ATOM 513 O LYS A 64 −10.062 −20.276 14.385 1.00 29.12 A O ATOM 514 CB LYS A 64 −12.016 −18.358 16.331 1.00 36.49 A C ATOM 515 CG LYS A 64 −12.829 −18.456 17.611 1.00 43.90 A C ATOM 516 CD LYS A 64 −14.061 −17.571 17.552 1.00 45.07 A C ATOM 517 CE LYS A 64 −14.886 −17.686 18.824 1.00 46.12 A C ATOM 518 NZ LYS A 64 −15.996 −16.690 18.845 1.00 53.34 A N ATOM 519 N VAL A 65 −9.524 −18.091 14.504 1.00 37.32 A N ATOM 520 CA VAL A 65 −8.883 −18.071 13.194 1.00 34.82 A C ATOM 521 C VAL A 65 −7.770 −19.110 13.153 1.00 34.94 A C ATOM 522 O VAL A 65 −7.611 −19.830 12.163 1.00 32.76 A O ATOM 523 CB VAL A 65 −8.287 −16.687 12.863 1.00 33.26 A C ATOM 524 CG1 VAL A 65 −7.703 −16.687 11.461 1.00 25.32 A C ATOM 525 CG2 VAL A 65 −9.337 −15.602 13.000 1.00 31.07 A C ATOM 526 N LEU A 66 −7.013 −19.191 14.245 1.00 33.50 A N ATOM 527 CA LEU A 66 −5.907 −20.131 14.346 1.00 34.39 A C ATOM 528 C LEU A 66 −6.369 −21.582 14.224 1.00 43.02 A C ATOM 529 O LEU A 66 −5.812 −22.356 13.437 1.00 40.25 A O ATOM 530 CB LEU A 66 −5.142 −19.924 15.653 1.00 37.57 A C ATOM 531 CG LEU A 66 −4.360 −18.614 15.753 1.00 41.06 A C ATOM 532 CD1 LEU A 66 −3.493 −18.610 16.994 1.00 40.01 A C ATOM 533 CD2 LEU A 66 −3.513 −18.409 14.508 1.00 34.50 A C ATOM 534 N LEU A 67 −7.385 −21.950 14.998 1.00 44.58 A N ATOM 535 CA LEU A 67 −7.897 −23.315 14.961 1.00 45.52 A C ATOM 536 C LEU A 67 −8.462 −23.658 13.590 1.00 44.52 A C ATOM 537 O LEU A 67 −8.327 −24.782 13.122 1.00 46.24 A O ATOM 538 CB LEU A 67 −8.947 −23.542 16.051 1.00 49.95 A C ATOM 539 CG LEU A 67 −8.367 −23.854 17.434 1.00 58.40 A C ATOM 540 CD1 LEU A 67 −9.474 −24.163 18.430 1.00 62.44 A C ATOM 541 CD2 LEU A 67 −7.373 −25.009 17.354 1.00 52.35 A C ATOM 542 N LYS A 68 −9.087 −22.677 12.951 1.00 28.77 A N ATOM 543 CA LYS A 68 −9.634 −22.855 11.616 1.00 30.29 A C ATOM 544 C LYS A 68 −8.490 −23.109 10.637 1.00 33.93 A C ATOM 545 O LYS A 68 −8.659 −23.794 9.624 1.00 33.71 A O ATOM 546 CB LYS A 68 −10.441 −21.616 11.218 1.00 32.94 A C ATOM 547 CG LYS A 68 −11.349 −21.788 10.010 1.00 35.71 A C ATOM 548 CD LYS A 68 −12.588 −20.911 10.149 1.00 33.52 A C ATOM 549 CE LYS A 68 −13.498 −21.001 8.930 1.00 31.15 A C ATOM 550 NZ LYS A 68 −13.079 −20.050 7.866 1.00 35.48 A N ATOM 551 N TYR A 69 −7.321 −22.563 10.959 1.00 40.79 A N ATOM 552 CA TYR A 69 −6.119 −22.772 10.155 1.00 42.75 A C ATOM 553 C TYR A 69 −5.551 −24.177 10.350 1.00 43.67 A C ATOM 554 O TYR A 69 −5.195 −24.849 9.381 1.00 39.63 A O ATOM 555 CB TYR A 69 −5.049 −21.726 10.495 1.00 35.20 A C ATOM 556 CG TYR A 69 −3.719 −21.966 9.812 1.00 29.77 A C ATOM 557 CD1 TYR A 69 −3.504 −21.552 8.504 1.00 30.89 A C ATOM 558 CD2 TYR A 69 −2.682 −22.608 10.472 1.00 31.32 A C ATOM 559 CE1 TYR A 69 −2.295 −21.768 7.875 1.00 27.04 A C ATOM 560 CE2 TYR A 69 −1.465 −22.831 9.848 1.00 28.93 A C ATOM 561 CZ TYR A 69 −1.280 −22.409 8.550 1.00 29.92 A C ATOM 562 OH TYR A 69 −0.075 −22.628 7.922 1.00 31.31 A O ATOM 563 N THR A 70 −5.459 −24.613 11.605 1.00 36.69 A N ATOM 564 CA THR A 70 −4.898 −25.928 11.906 1.00 43.59 A C ATOM 565 C THR A 70 −5.838 −27.048 11.470 1.00 45.00 A C ATOM 566 O THR A 70 −5.397 −28.043 10.894 1.00 48.92 A O ATOM 567 CB THR A 70 −4.529 −26.084 13.403 1.00 41.16 A C ATOM 568 OG1 THR A 70 −5.627 −25.665 14.221 1.00 56.03 A O ATOM 569 CG2 THR A 70 −3.305 −25.240 13.741 1.00 41.46 A C ATOM 570 N GLU A 71 −7.130 −26.877 11.732 1.00 71.37 A N ATOM 571 CA GLU A 71 −8.130 −27.853 11.308 1.00 82.63 A C ATOM 572 C GLU A 71 −8.173 −27.949 9.786 1.00 76.61 A C ATOM 573 O GLU A 71 −8.610 −28.954 9.229 1.00 81.40 A O ATOM 574 CB GLU A 71 −9.521 −27.478 11.838 1.00 78.47 A C ATOM 575 CG GLU A 71 −9.607 −27.275 13.348 1.00 86.35 A C ATOM 576 CD GLU A 71 −9.479 −28.566 14.132 1.00 90.69 A C ATOM 577 OE1 GLU A 71 −9.615 −29.650 13.525 1.00 97.70 A O ATOM 578 OE2 GLU A 71 −9.249 −28.494 15.359 1.00 83.58 A O ATOM 579 N TYR A 72 −7.713 −26.894 9.120 1.00 49.20 A N ATOM 580 CA TYR A 72 −7.800 −26.799 7.667 1.00 47.92 A C ATOM 581 C TYR A 72 −7.085 −27.958 6.983 1.00 45.30 A C ATOM 582 O TYR A 72 −7.519 −28.423 5.930 1.00 42.68 A O ATOM 583 CB TYR A 72 −7.225 −25.464 7.187 1.00 44.29 A C ATOM 584 CG TYR A 72 −7.659 −25.054 5.794 1.00 41.13 A C ATOM 585 CD1 TYR A 72 −8.875 −24.416 5.586 1.00 35.47 A C ATOM 586 CD2 TYR A 72 −6.845 −25.291 4.689 1.00 43.90 A C ATOM 587 CE1 TYR A 72 −9.277 −24.030 4.316 1.00 34.32 A C ATOM 588 CE2 TYR A 72 −7.235 −24.906 3.414 1.00 38.74 A C ATOM 589 CZ TYR A 72 −8.453 −24.275 3.234 1.00 42.36 A C ATOM 590 OH TYR A 72 −8.852 −23.888 1.972 1.00 38.66 A O TER ATOM 591 N GLY B 2 −9.188 5.872 −5.539 1.00 35.93 B N ATOM 592 CA GLY B 2 −9.888 5.453 −6.741 1.00 41.50 B C ATOM 593 C GLY B 2 −10.704 6.574 −7.356 1.00 43.98 B C ATOM 594 O GLY B 2 −10.628 7.722 −6.907 1.00 39.60 B O ATOM 595 N ARG B 3 −11.484 6.244 −8.384 1.00 34.91 B N ATOM 596 CA ARG B 3 −12.303 7.235 −9.080 1.00 36.90 B C ATOM 597 C ARG B 3 −13.303 7.899 −8.138 1.00 39.43 B C ATOM 598 O ARG B 3 −13.661 9.065 −8.311 1.00 43.98 B O ATOM 599 CB ARG B 3 −13.029 6.601 −10.267 1.00 37.34 B C ATOM 600 CG ARG B 3 −12.101 6.102 −11.369 1.00 39.68 B C ATOM 601 CD ARG B 3 −11.130 7.187 −11.823 1.00 42.23 B C ATOM 602 NE ARG B 3 −10.365 6.783 −13.000 1.00 38.79 B N ATOM 603 CZ ARG B 3 −10.840 6.808 −14.242 1.00 44.35 B C ATOM 604 NH1 ARG B 3 −12.084 7.212 −14.474 1.00 33.55 B N ATOM 605 NH2 ARG B 3 −10.073 6.423 −15.253 1.00 43.80 B N ATOM 606 N LYS B 4 −13.753 7.144 −7.143 1.00 32.66 B N ATOM 607 CA LYS B 4 −14.606 7.679 −6.094 1.00 32.76 B C ATOM 608 C LYS B 4 −14.195 7.094 −4.752 1.00 36.67 B C ATOM 609 O LYS B 4 −13.841 5.915 −4.658 1.00 31.80 B O ATOM 610 CB LYS B 4 −16.075 7.341 −6.357 1.00 35.54 B C ATOM 611 CG LYS B 4 −16.670 7.976 −7.605 1.00 39.71 B C ATOM 612 CD LYS B 4 −18.000 7.320 −7.949 1.00 35.56 B C ATOM 613 CE LYS B 4 −18.425 7.630 −9.371 1.00 47.36 B C ATOM 614 NZ LYS B 4 −19.420 6.635 −9.876 1.00 51.32 B N ATOM 615 N LYS B 5 −14.235 7.922 −3.716 1.00 40.04 B N ATOM 616 CA LYS B 5 −14.081 7.426 −2.362 1.00 37.87 B C ATOM 617 C LYS B 5 −15.249 6.499 −2.081 1.00 39.79 B C ATOM 618 O LYS B 5 −16.384 6.802 −2.449 1.00 40.95 B O ATOM 619 CB LYS B 5 −14.082 8.583 −1.359 1.00 35.44 B C ATOM 620 CG LYS B 5 −14.292 8.145 0.087 1.00 40.32 B C ATOM 621 CD LYS B 5 −13.906 9.244 1.069 1.00 36.82 B C ATOM 622 CE LYS B 5 −13.884 8.717 2.494 1.00 46.24 B C ATOM 623 NZ LYS B 5 −13.497 9.771 3.476 1.00 52.66 B N ATOM 624 N ILE B 6 −14.972 5.363 −1.449 1.00 39.51 B N ATOM 625 CA ILE B 6 −16.037 4.465 −1.020 1.00 39.10 B C ATOM 626 C ILE B 6 −16.194 4.479 0.495 1.00 44.95 B C ATOM 627 O ILE B 6 −15.428 5.129 1.207 1.00 43.30 B O ATOM 628 CB ILE B 6 −15.795 3.017 −1.473 1.00 43.66 B C ATOM 629 CG1 ILE B 6 −14.604 2.411 −0.728 1.00 41.77 B C ATOM 630 CG2 ILE B 6 −15.606 2.954 −2.982 1.00 47.69 B C ATOM 631 CD1 ILE B 6 −14.433 0.923 −0.970 1.00 39.73 B C ATOM 632 N GLN B 7 −17.203 3.765 0.977 1.00 36.28 B N ATOM 633 CA GLN B 7 −17.422 3.616 2.405 1.00 37.59 B C ATOM 634 C GLN B 7 −17.066 2.196 2.786 1.00 33.90 B C ATOM 635 O GLN B 7 −17.264 1.269 2.000 1.00 33.84 B O ATOM 636 CB GLN B 7 −18.880 3.911 2.765 1.00 47.49 B C ATOM 637 CG GLN B 7 −19.228 5.391 2.796 1.00 45.21 B C ATOM 638 CD GLN B 7 −18.721 6.085 4.048 1.00 62.62 B C ATOM 639 OE1 GLN B 7 −19.133 5.760 5.164 1.00 65.96 B O ATOM 640 NE2 GLN B 7 −17.829 7.054 3.866 1.00 64.78 B N ATOM 641 N ILE B 8 −16.534 2.025 3.990 1.00 28.89 B N ATOM 642 CA ILE B 8 −16.087 0.712 4.435 1.00 24.06 B C ATOM 643 C ILE B 8 −17.257 −0.135 4.929 1.00 26.92 B C ATOM 644 O ILE B 8 −17.536 −0.209 6.128 1.00 26.19 B O ATOM 645 CB ILE B 8 −14.965 0.823 5.495 1.00 20.79 B C ATOM 646 CG1 ILE B 8 −13.755 1.528 4.882 1.00 20.90 B C ATOM 647 CG2 ILE B 8 −14.556 −0.546 6.017 1.00 18.34 B C ATOM 648 CD1 ILE B 8 −13.387 1.003 3.506 1.00 20.40 B C ATOM 649 N THR B 9 −17.947 −0.767 3.984 1.00 28.04 B N ATOM 650 CA THR B 9 −19.038 −1.677 4.313 1.00 28.46 B C ATOM 651 C THR B 9 −19.055 −2.860 3.344 1.00 24.67 B C ATOM 652 O THR B 9 −18.658 −2.724 2.186 1.00 28.00 B O ATOM 653 CB THR B 9 −20.399 −0.949 4.311 1.00 34.72 B C ATOM 654 OG1 THR B 9 −21.408 −1.809 4.860 1.00 36.57 B O ATOM 655 CG2 THR B 9 −20.784 −0.520 2.894 1.00 26.37 B C ATOM 656 N ARG B 10 −19.502 −4.015 3.830 1.00 23.22 B N ATOM 657 CA ARG B 10 −19.521 −5.249 3.041 1.00 27.96 B C ATOM 658 C ARG B 10 −20.109 −5.073 1.644 1.00 27.22 B C ATOM 659 O ARG B 10 −21.267 −4.682 1.491 1.00 29.90 B O ATOM 660 CB ARG B 10 −20.283 −6.353 3.777 1.00 27.06 B C ATOM 661 CG ARG B 10 −20.326 −7.678 3.024 1.00 27.66 B C ATOM 662 CD ARG B 10 −21.227 −8.687 3.728 1.00 30.60 B C ATOM 663 NE ARG B 10 −21.283 −9.974 3.035 1.00 44.23 B N ATOM 664 CZ ARG B 10 −22.086 −10.242 2.007 1.00 41.38 B C ATOM 665 NH1 ARG B 10 −22.905 −9.309 1.539 1.00 42.70 B N ATOM 666 NH2 ARG B 10 −22.070 −11.443 1.442 1.00 34.97 B N ATOM 667 N ILE B 11 −19.299 −5.367 0.632 1.00 18.77 B N ATOM 668 CA ILE B 11 −19.735 −5.298 −0.756 1.00 19.25 B C ATOM 669 C ILE B 11 −20.735 −6.417 −1.041 1.00 25.50 B C ATOM 670 O ILE B 11 −20.462 −7.592 −0.773 1.00 23.75 B O ATOM 671 CB ILE B 11 −18.539 −5.406 −1.714 1.00 20.42 B C ATOM 672 CG1 ILE B 11 −17.639 −4.181 −1.565 1.00 15.67 B C ATOM 673 CG2 ILE B 11 −19.009 −5.539 −3.154 1.00 18.62 B C ATOM 674 CD1 ILE B 11 −16.254 −4.380 −2.103 1.00 17.71 B C ATOM 675 N MET B 12 −21.893 −6.047 −1.579 1.00 22.51 B N ATOM 676 CA MET B 12 −23.000 −6.985 −1.720 1.00 24.87 B C ATOM 677 C MET B 12 −22.909 −7.816 −2.996 1.00 31.08 B C ATOM 678 O MET B 12 −23.373 −8.955 −3.032 1.00 25.68 B O ATOM 679 CB MET B 12 −24.341 −6.246 −1.657 1.00 25.38 B C ATOM 680 CG MET B 12 −24.564 −5.470 −0.358 1.00 30.39 B C ATOM 681 SD MET B 12 −24.573 −6.517 1.118 1.00 35.66 B S ATOM 682 CE MET B 12 −26.117 −7.406 0.874 1.00 22.73 B C ATOM 683 N ASP B 13 −22.315 −7.242 −4.039 1.00 38.07 B N ATOM 684 CA ASP B 13 −22.152 −7.942 −5.311 1.00 39.19 B C ATOM 685 C ASP B 13 −20.988 −8.931 −5.246 1.00 41.47 B C ATOM 686 O ASP B 13 −19.841 −8.536 −5.025 1.00 36.72 B O ATOM 687 CB ASP B 13 −21.925 −6.939 −6.448 1.00 39.47 B C ATOM 688 CG ASP B 13 −21.667 −7.617 −7.790 1.00 59.19 B C ATOM 689 OD1 ASP B 13 −22.367 −8.603 −8.109 1.00 58.53 B O ATOM 690 OD2 ASP B 13 −20.767 −7.158 −8.530 1.00 56.17 B O ATOM 691 N GLU B 14 −21.290 −10.212 −5.433 1.00 29.13 B N ATOM 692 CA GLU B 14 −20.272 −11.262 −5.425 1.00 30.70 B C ATOM 693 C GLU B 14 −19.154 −10.996 −6.431 1.00 35.92 B C ATOM 694 O GLU B 14 −17.984 −11.262 −6.157 1.00 32.47 B O ATOM 695 CB GLU B 14 −20.906 −12.622 −5.718 1.00 29.50 B C ATOM 696 CG GLU B 14 −19.928 −13.785 −5.799 1.00 35.92 B C ATOM 697 CD GLU B 14 −20.584 −15.052 −6.339 1.00 61.30 B C ATOM 698 OE1 GLU B 14 −21.212 −14.986 −7.421 1.00 65.75 B O ATOM 699 OE2 GLU B 14 −20.475 −16.112 −5.683 1.00 53.89 B O ATOM 700 N ARG B 15 −19.511 −10.473 −7.597 1.00 46.25 B N ATOM 701 CA ARG B 15 −18.516 −10.214 −8.631 1.00 39.81 B C ATOM 702 C ARG B 15 −17.541 −9.116 −8.215 1.00 34.94 B C ATOM 703 O ARG B 15 −16.337 −9.348 −8.165 1.00 30.98 B O ATOM 704 CB ARG B 15 −19.184 −9.880 −9.965 1.00 47.87 B C ATOM 705 CG ARG B 15 −18.255 −9.253 −10.988 1.00 53.75 B C ATOM 706 CD ARG B 15 −18.624 −9.678 −12.403 1.00 61.36 B C ATOM 707 NE ARG B 15 −18.159 −11.032 −12.697 1.00 67.24 B N ATOM 708 CZ ARG B 15 −18.907 −12.127 −12.584 1.00 69.40 B C ATOM 709 NH1 ARG B 15 −20.170 −12.036 −12.188 1.00 74.25 B N ATOM 710 NH2 ARG B 15 −18.389 −13.317 −12.873 1.00 47.80 B N ATOM 711 N ASN B 16 −18.057 −7.927 −7.916 1.00 38.39 B N ATOM 712 CA ASN B 16 −17.201 −6.832 −7.467 1.00 33.29 B C ATOM 713 C ASN B 16 −16.510 −7.157 −6.144 1.00 30.20 B C ATOM 714 O ASN B 16 −15.475 −6.580 −5.820 1.00 31.16 B O ATOM 715 CB ASN B 16 −17.980 −5.514 −7.344 1.00 38.21 B C ATOM 716 CG ASN B 16 −17.124 −4.371 −6.764 1.00 48.55 B C ATOM 717 OD1 ASN B 16 −15.983 −4.145 −7.190 1.00 31.35 B O ATOM 718 ND2 ASN B 16 −17.681 −3.646 −5.790 1.00 34.92 B N ATOM 719 N ARG B 17 −17.079 −8.077 −5.374 1.00 21.31 B N ATOM 720 CA ARG B 17 −16.484 −8.412 −4.091 1.00 25.28 B C ATOM 721 C ARG B 17 −15.244 −9.251 −4.316 1.00 27.07 B C ATOM 722 O ARG B 17 −14.212 −9.041 −3.675 1.00 27.84 B O ATOM 723 CB ARG B 17 −17.464 −9.151 −3.184 1.00 24.01 B C ATOM 724 CG ARG B 17 −16.867 −9.515 −1.834 1.00 23.82 B C ATOM 725 CD ARG B 17 −17.926 −9.981 −0.842 1.00 26.00 B C ATOM 726 NE ARG B 17 −18.536 −11.237 −1.258 1.00 32.53 B N ATOM 727 CZ ARG B 17 −19.797 −11.363 −1.661 1.00 33.84 B C ATOM 728 NH1 ARG B 17 −20.604 −10.306 −1.687 1.00 26.61 B N ATOM 729 NH2 ARG B 17 −20.251 −12.553 −2.031 1.00 33.93 B N ATOM 730 N GLN B 18 −15.350 −10.202 −5.236 1.00 29.00 B N ATOM 731 CA GLN B 18 −14.225 −11.058 −5.573 1.00 30.09 B C ATOM 732 C GLN B 18 −13.091 −10.247 −6.192 1.00 25.53 B C ATOM 733 O GLN B 18 −11.921 −10.457 −5.868 1.00 22.89 B O ATOM 734 CB GLN B 18 −14.669 −12.182 −6.513 1.00 28.95 B C ATOM 735 CG GLN B 18 −13.522 −12.988 −7.104 1.00 29.28 B C ATOM 736 CD GLN B 18 −12.610 −13.585 −6.048 1.00 33.30 B C ATOM 737 OE1 GLN B 18 −12.886 −13.510 −4.850 1.00 38.50 B O ATOM 738 NE2 GLN B 18 −11.508 −14.184 −6.492 1.00 42.99 B N ATOM 739 N VAL B 19 −13.448 −9.313 −7.070 1.00 25.06 B N ATOM 740 CA VAL B 19 −12.472 −8.442 −7.718 1.00 28.61 B C ATOM 741 C VAL B 19 −11.723 −7.571 −6.710 1.00 29.35 B C ATOM 742 O VAL B 19 −10.495 −7.502 −6.728 1.00 30.32 B O ATOM 743 CB VAL B 19 −13.136 −7.529 −8.765 1.00 27.95 B C ATOM 744 CG1 VAL B 19 −12.285 −6.291 −9.013 1.00 28.44 B C ATOM 745 CG2 VAL B 19 −13.361 −8.288 −10.053 1.00 31.41 B C ATOM 746 N THR B 20 −12.469 −6.905 −5.836 1.00 28.91 B N ATOM 747 CA THR B 20 −11.866 −6.061 −4.815 1.00 26.07 B C ATOM 748 C THR B 20 −11.017 −6.903 −3.875 1.00 27.75 B C ATOM 749 O THR B 20 −9.937 −6.488 −3.453 1.00 24.01 B O ATOM 750 CB THR B 20 −12.928 −5.306 −4.012 1.00 27.80 B C ATOM 751 OG1 THR B 20 −13.454 −4.244 −4.814 1.00 29.96 B O ATOM 752 CG2 THR B 20 −12.324 −4.722 −2.735 1.00 24.77 B C ATOM 753 N PHE B 21 −11.503 −8.096 −3.556 1.00 22.15 B N ATOM 754 CA PHE B 21 −10.746 −8.998 −2.698 1.00 21.89 B C ATOM 755 C PHE B 21 −9.365 −9.324 −3.272 1.00 18.93 B C ATOM 756 O PHE B 21 −8.367 −9.306 −2.553 1.00 19.66 B O ATOM 757 CB PHE B 21 −11.523 −10.287 −2.446 1.00 19.40 B C ATOM 758 CG PHE B 21 −10.707 −11.361 −1.796 1.00 19.58 B C ATOM 759 CD1 PHE B 21 −10.525 −11.374 −0.424 1.00 17.26 B C ATOM 760 CD2 PHE B 21 −10.116 −12.353 −2.557 1.00 19.84 B C ATOM 761 CE1 PHE B 21 −9.774 −12.358 0.180 1.00 20.45 B C ATOM 762 CE2 PHE B 21 −9.360 −13.343 −1.960 1.00 22.00 B C ATOM 763 CZ PHE B 21 −9.190 −13.348 −0.589 1.00 28.35 B C ATOM 764 N THR B 22 −9.312 −9.628 −4.563 1.00 21.88 B N ATOM 765 CA THR B 22 −8.054 −9.996 −5.202 1.00 20.53 B C ATOM 766 C THR B 22 −7.093 −8.808 −5.230 1.00 19.42 B C ATOM 767 O THR B 22 −5.899 −8.960 −4.967 1.00 20.21 B O ATOM 768 CB THR B 22 −8.267 −10.561 −6.640 1.00 24.17 B C ATOM 769 OG1 THR B 22 −8.869 −11.862 −6.570 1.00 23.68 B O ATOM 770 CG2 THR B 22 −6.945 −10.675 −7.377 1.00 15.72 B C ATOM 771 N LYS B 23 −7.607 −7.622 −5.542 1.00 17.48 B N ATOM 772 CA LYS B 23 −6.756 −6.437 −5.542 1.00 19.24 B C ATOM 773 C LYS B 23 −6.181 −6.175 −4.149 1.00 18.39 B C ATOM 774 O LYS B 23 −4.962 −6.144 −3.971 1.00 18.07 B O ATOM 775 CB LYS B 23 −7.511 −5.203 −6.050 1.00 20.59 B C ATOM 776 CG LYS B 23 −7.846 −5.236 −7.535 1.00 26.67 B C ATOM 777 CD LYS B 23 −8.583 −3.964 −7.961 1.00 28.62 B C ATOM 778 CE LYS B 23 −8.978 −4.026 −9.431 1.00 28.02 B C ATOM 779 NZ LYS B 23 −9.916 −2.935 −9.814 1.00 32.81 B N ATOM 780 N ARG B 24 −7.061 −6.009 −3.165 1.00 16.09 B N ATOM 781 CA ARG B 24 −6.640 −5.635 −1.812 1.00 16.07 B C ATOM 782 C ARG B 24 −5.836 −6.711 −1.072 1.00 18.15 B C ATOM 783 O ARG B 24 −5.008 −6.378 −0.218 1.00 15.59 B O ATOM 784 CB ARG B 24 −7.832 −5.174 −0.969 1.00 13.10 B C ATOM 785 CG ARG B 24 −8.234 −3.717 −1.203 1.00 14.76 B C ATOM 786 CD ARG B 24 −9.495 −3.357 −0.424 1.00 14.27 B C ATOM 787 NE ARG B 24 −9.879 −1.954 −0.584 1.00 15.73 B N ATOM 788 CZ ARG B 24 −9.536 −0.980 0.258 1.00 18.12 B C ATOM 789 NH1 ARG B 24 −8.797 −1.247 1.331 1.00 16.01 B N ATOM 790 NH2 ARG B 24 −9.933 0.263 0.028 1.00 16.88 B N ATOM 791 N LYS B 25 −6.064 −7.987 −1.394 1.00 19.04 B N ATOM 792 CA LYS B 25 −5.278 −9.061 −0.779 1.00 19.08 B C ATOM 793 C LYS B 25 −3.822 −8.901 −1.164 1.00 18.45 B C ATOM 794 O LY5 B 25 −2.930 −8.970 −0.328 1.00 19.20 B O ATOM 795 CB LYS B 25 −5.762 −10.447 −1.214 1.00 23.30 B C ATOM 796 CG LYS B 25 −4.782 −11.570 −0.853 1.00 19.47 B C ATOM 797 CD LYS B 25 −5.469 −12.936 −0.772 1.00 22.91 B C ATOM 798 CE LYS B 25 −5.988 −13.411 −2.138 1.00 26.31 B C ATOM 799 NZ LYS B 25 −4.897 −13.779 −3.087 1.00 20.74 B N ATOM 800 N PHE B 26 −3.594 −8.692 −2.451 1.00 16.72 B N ATOM 801 CA PHE B 26 −2.260 −8.430 −2.954 1.00 17.53 B C ATOM 802 C PHE B 26 −1.655 −7.216 −2.226 1.00 19.47 B C ATOM 803 O PHE B 26 −0.552 −7.285 −1.684 1.00 20.99 B O ATOM 804 CB PHE B 26 −2.336 −8.184 −4.460 1.00 17.86 B C ATOM 805 CG PHE B 26 −1.008 −8.004 −5.109 1.00 21.69 B C ATOM 806 CD1 PHE B 26 −0.379 −9.073 −5.732 1.00 25.97 B C ATOM 807 CD2 PHE B 26 −0.386 −6.768 −5.110 1.00 18.89 B C ATOM 808 CE1 PHE B 26 0.853 −8.913 −6.342 1.00 25.80 B C ATOM 809 CE2 PHE B 26 0.848 −6.602 −5.718 1.00 25.93 B C ATOM 810 CZ PHE B 26 1.467 −7.676 −6.333 1.00 23.95 B C ATOM 811 N GLY B 27 −2.395 −6.111 −2.213 1.00 19.53 B N ATOM 812 CA GLY B 27 −1.966 −4.896 −1.548 1.00 18.26 B C ATOM 813 C GLY B 27 −1.679 −5.073 −0.069 1.00 17.11 B C ATOM 814 O GLY B 27 −0.796 −4.415 0.474 1.00 15.96 B O ATOM 815 N LEU B 28 −2.423 −5.959 0.589 1.00 18.00 B N ATOM 816 CA LEU B 28 −2.214 −6.213 2.016 1.00 18.51 B C ATOM 817 C LEU B 28 −0.923 −6.999 2.259 1.00 18.19 B C ATOM 818 O LEU B 28 −0.141 −6.670 3.156 1.00 15.92 B O ATOM 819 CB LEU B 28 −3.406 −6.962 2.619 1.00 18.03 B C ATOM 820 CG LEU B 28 −3.321 −7.263 4.123 1.00 17.44 B C ATOM 821 CD1 LEU B 28 −3.250 −5.981 4.924 1.00 15.32 B C ATOM 822 CD2 LEU B 28 −4.506 −8.112 4.579 1.00 16.82 B C ATOM 823 N MET B 29 −0.710 −8.034 1.450 1.00 20.23 B N ATOM 824 CA MET B 29 0.502 −8.845 1.525 1.00 19.85 B C ATOM 825 C MET B 29 1.733 −8.013 1.190 1.00 17.85 B C ATOM 826 O MET B 29 2.770 −8.150 1.823 1.00 17.90 B O ATOM 827 CB MET B 29 0.410 −10.050 0.585 1.00 21.04 B C ATOM 828 CG MET B 29 −0.699 −11.045 0.936 1.00 20.57 B C ATOM 829 SD MET B 29 −0.410 −12.688 0.227 1.00 25.22 B S ATOM 830 CE MET B 29 −1.808 −13.585 0.911 1.00 25.68 B C ATOM 831 N LYS B 30 1.612 −7.141 0.198 1.00 21.15 B N ATOM 832 CA LYS B 30 2.733 −6.297 −0.199 1.00 23.46 B C ATOM 833 C LYS B 30 3.208 −5.420 0.963 1.00 22.21 B C ATOM 834 O LYS B 30 4.409 −5.327 1.230 1.00 22.98 B O ATOM 835 CB LYS B 30 2.380 −5.439 −1.418 1.00 22.85 B C ATOM 836 CG LYS B 30 3.597 −4.786 −2.066 1.00 31.19 B C ATOM 837 CD LYS B 30 3.233 −3.940 −3.284 1.00 30.28 B C ATOM 838 CE LYS B 30 4.410 −3.069 −3.708 1.00 32.21 B C ATOM 839 NZ LYS B 30 3.999 −1.884 −4.515 1.00 32.92 B N ATOM 840 N LYS B 31 2.269 −4.785 1.661 1.00 18.51 B N ATOM 841 CA LYS B 31 2.629 −3.953 2.810 1.00 19.94 B C ATOM 842 C LYS B 31 3.135 −4.774 4.002 1.00 17.10 B C ATOM 843 O LYS B 31 4.045 −4.354 4.707 1.00 19.53 B O ATOM 844 CB LYS B 31 1.474 −3.025 3.202 1.00 16.96 B C ATOM 845 CG LYS B 31 1.285 −1.885 2.214 1.00 16.08 B C ATOM 846 CD LYS B 31 0.282 −0.855 2.704 1.00 22.23 B C ATOM 847 CE LYS B 31 0.246 0.355 1.779 1.00 22.27 B C ATOM 848 NZ LYS B 31 1.595 0.974 1.641 1.00 23.12 B N ATOM 849 N ALA B 32 2.560 −5.953 4.206 1.00 11.50 B N ATOM 850 CA ALA B 32 3.033 −6.860 5.242 1.00 12.27 B C ATOM 851 C ALA B 32 4.503 −7.208 4.998 1.00 15.88 B C ATOM 852 O ALA B 32 5.327 −7.137 5.913 1.00 13.80 B O ATOM 853 CB ALA B 32 2.182 −8.123 5.269 1.00 11.97 B C ATOM 854 N TYR B 33 4.819 −7.581 3.757 1.00 22.53 B N ATOM 855 CA TYR B 33 6.189 −7.880 3.346 1.00 21.55 B C ATOM 856 C TYR B 33 7.141 −6.692 3.554 1.00 23.48 B C ATOM 857 O TYR B 33 8.224 −6.843 4.124 1.00 24.87 B O ATOM 858 CB TYR B 33 6.214 −8.336 1.880 1.00 26.95 B C ATOM 859 CG TYR B 33 7.560 −8.179 1.202 1.00 25.09 B C ATOM 860 CD1 TYR B 33 8.596 −9.064 1.460 1.00 27.42 B C ATOM 861 CD2 TYR B 33 7.794 −7.140 0.306 1.00 25.48 B C ATOM 862 CE1 TYR B 33 9.831 −8.922 0.848 1.00 29.33 B C ATOM 863 CE2 TYR B 33 9.027 −6.986 −0.308 1.00 25.23 B C ATOM 864 CZ TYR B 33 10.040 −7.881 −0.033 1.00 29.66 B C ATOM 865 OH TYR B 33 11.269 −7.743 −0.642 1.00 32.89 B O ATOM 866 N GLU B 34 6.735 −5.517 3.086 1.00 17.81 B N ATOM 867 CA GLU B 34 7.539 −4.308 3.231 1.00 19.60 B C ATOM 868 C GLU B 34 7.810 −3.965 4.696 1.00 20.91 B C ATOM 869 O GLU B 34 8.931 −3.579 5.054 1.00 17.67 B O ATOM 870 CB GLU B 34 6.876 −3.126 2.518 1.00 18.42 B C ATOM 871 CG GLU B 34 6.846 −3.262 0.997 1.00 19.82 B C ATOM 872 CD GLU B 34 6.199 −2.067 0.310 1.00 25.58 B C ATOM 873 OE1 GLU B 34 5.545 −1.255 1.004 1.00 22.87 B O ATOM 874 OE2 GLU B 34 6.345 −1.939 −0.926 1.00 21.30 B O ATOM 875 N LEU B 35 6.793 −4.115 5.544 1.00 16.91 B N ATOM 876 CA LEU B 35 6.966 −3.847 6.972 1.00 16.29 B C ATOM 877 C LEU B 35 7.932 −4.845 7.619 1.00 16.61 B C ATOM 878 O LEU B 35 8.731 −4.482 8.487 1.00 18.25 B O ATOM 879 CB LEU B 35 5.626 −3.850 7.708 1.00 13.34 B C ATOM 880 CG LEU B 35 5.763 −3.654 9.219 1.00 14.59 B C ATOM 881 CD1 LEU B 35 6.310 −2.272 9.516 1.00 14.93 B C ATOM 882 CD2 LEU B 35 4.451 −3.882 9.940 1.00 14.02 B C ATOM 883 N SER B 36 7.860 −6.102 7.204 1.00 17.19 B N ATOM 884 CA SER B 36 8.792 −7.102 7.716 1.00 26.25 B C ATOM 885 C SER B 36 10.251 −6.770 7.364 1.00 21.13 B C ATOM 886 O SER B 36 11.153 −6.935 8.183 1.00 23.34 B O ATOM 887 CB SER B 36 8.431 −8.494 7.199 1.00 23.09 B C ATOM 888 OG SER B 36 9.402 −9.438 7.616 1.00 27.07 B O ATOM 889 N VAL B 37 10.473 −6.299 6.143 1.00 20.97 B N ATOM 890 CA VAL B 37 11.820 −5.988 5.678 1.00 21.94 B C ATOM 891 C VAL B 37 12.328 −4.665 6.247 1.00 22.41 B C ATOM 892 O VAL B 37 13.440 −4.588 6.769 1.00 22.46 B O ATOM 893 CB VAL B 37 11.877 −5.935 4.139 1.00 21.78 B C ATOM 894 CG1 VAL B 37 13.164 −5.273 3.667 1.00 17.34 B C ATOM 895 CG2 VAL B 37 11.742 −7.336 3.562 1.00 22.73 B C ATOM 896 N LEU B 38 11.509 −3.625 6.139 1.00 29.65 B N ATOM 897 CA LEU B 38 11.895 −2.302 6.606 1.00 29.22 B C ATOM 898 C LEU B 38 12.222 −2.292 8.095 1.00 29.43 B C ATOM 899 O LEU B 38 13.176 −1.639 8.527 1.00 29.26 B O ATOM 900 CB LEU B 38 10.781 −1.294 6.326 1.00 27.68 B C ATOM 901 CG LEU B 38 10.564 −0.877 4.875 1.00 27.08 B C ATOM 902 CD1 LEU B 38 9.277 −0.077 4.758 1.00 23.22 B C ATOM 903 CD2 LEU B 38 11.756 −0.083 4.363 1.00 24.95 B C ATOM 904 N CYS B 39 11.432 −3.015 8.880 1.00 17.61 B N ATOM 905 CA CYS B 39 11.579 −2.941 10.330 1.00 22.07 B C ATOM 906 C CYS B 39 12.059 −4.238 10.992 1.00 21.34 B C ATOM 907 O CYS B 39 12.094 −4.338 12.216 1.00 24.49 B O ATOM 908 CB CYS B 39 10.276 −2.448 10.968 1.00 15.92 B C ATOM 909 SG CYS B 39 9.701 −0.901 10.239 1.00 19.75 B S ATOM 910 N ASP B 40 12.433 −5.226 10.191 1.00 31.69 B N ATOM 911 CA ASP B 40 12.981 −6.454 10.754 1.00 37.68 B C ATOM 912 C ASP B 40 12.040 −7.040 11.810 1.00 37.06 B C ATOM 913 O ASP B 40 12.325 −6.975 13.006 1.00 34.46 B O ATOM 914 CB ASP B 40 14.351 −6.169 11.382 1.00 33.34 B C ATOM 915 CG ASP B 40 15.076 −7.432 11.824 1.00 41.25 B C ATOM 916 OD1 ASP B 40 14.704 −8.540 11.380 1.00 43.90 B O ATOM 917 OD2 ASP B 40 16.031 −7.312 12.621 1.00 52.43 B O ATOM 918 N CYS B 41 10.919 −7.603 11.370 1.00 28.73 B N ATOM 919 CA CYS B 41 9.996 −8.257 12.289 1.00 33.22 B C ATOM 920 C CYS B 41 9.336 −9.506 11.693 1.00 31.42 B C ATOM 921 O CYS B 41 9.191 −9.620 10.477 1.00 31.49 B O ATOM 922 CB CYS B 41 8.943 −7.266 12.798 1.00 30.60 B C ATOM 923 SG CYS B 41 8.329 −6.093 11.583 1.00 39.58 B S ATOM 924 N GLU B 42 8.966 −10.446 12.561 1.00 32.53 B N ATOM 925 CA GLU B 42 8.232 −11.638 12.153 1.00 34.28 B C ATOM 926 C GLU B 42 6.772 −11.284 11.955 1.00 31.82 B C ATOM 927 O GLU B 42 6.133 −10.739 12.853 1.00 32.57 B O ATOM 928 CB GLU B 42 8.303 −12.725 13.225 1.00 36.20 B C ATOM 929 CG GLU B 42 9.646 −13.393 13.405 1.00 46.15 B C ATOM 930 CD GLU B 42 9.568 −14.549 14.382 1.00 47.22 B C ATOM 931 OE1 GLU B 42 10.523 −14.734 15.167 1.00 64.02 B O ATOM 932 OE2 GLU B 42 8.542 −15.265 14.372 1.00 37.09 B O ATOM 933 N ILE B 43 6.232 −11.615 10.792 1.00 20.98 B N ATOM 934 CA ILE B 43 4.832 −11.335 10.524 1.00 20.90 B C ATOM 935 C ILE B 43 4.116 −12.561 9.975 1.00 20.19 B C ATOM 936 O ILE B 43 4.693 −13.344 9.223 1.00 21.90 B O ATOM 937 CB ILE B 43 4.678 −10.128 9.578 1.00 21.58 B C ATOM 938 CG1 ILE B 43 5.102 −8.848 10.310 1.00 18.84 B C ATOM 939 CG2 ILE B 43 3.244 −10.033 9.056 1.00 14.53 B C ATOM 940 CD1 ILE B 43 5.145 −7.608 9.446 1.00 16.56 B C ATOM 941 N ALA B 44 2.865 −12.735 10.381 1.00 22.30 B N ATOM 942 CA ALA B 44 2.028 −13.807 9.861 1.00 22.53 B C ATOM 943 C ALA B 44 0.660 −13.234 9.523 1.00 20.25 B C ATOM 944 O ALA B 44 0.123 −12.420 10.266 1.00 22.18 B O ATOM 945 CB ALA B 44 1.907 −14.946 10.878 1.00 20.13 B C ATOM 946 N LEU B 45 0.102 −13.660 8.398 1.00 21.92 B N ATOM 947 CA LEU B 45 −1.165 −13.124 7.928 1.00 18.74 B C ATOM 948 C LEU B 45 −2.013 −14.241 7.342 1.00 22.81 B C ATOM 949 O LEU B 45 −1.791 −14.662 6.210 1.00 25.91 B O ATOM 950 CB LEU B 45 −0.908 −12.046 6.869 1.00 21.14 B C ATOM 951 CG LEU B 45 −2.098 −11.413 6.139 1.00 21.33 B C ATOM 952 CD1 LEU B 45 −3.034 −10.714 7.115 1.00 18.73 B C ATOM 953 CD2 LEU B 45 −1.623 −10.441 5.059 1.00 15.76 B C ATOM 954 N ILE B 46 −2.980 −14.726 8.112 1.00 28.56 B N ATOM 955 CA ILE B 46 −3.894 −15.759 7.627 1.00 28.46 B C ATOM 956 C ILE B 46 −5.221 −15.148 7.187 1.00 27.91 B C ATOM 957 O ILE B 46 −5.828 −14.367 7.922 1.00 28.37 B O ATOM 958 CB ILE B 46 −4.152 −16.829 8.704 1.00 29.75 B C ATOM 959 CG1 ILE B 46 −2.865 −17.601 8.999 1.00 27.86 B C ATOM 960 CG2 ILE B 46 −5.243 −17.774 8.258 1.00 29.11 B C ATOM 961 CD1 ILE B 46 −2.877 −18.332 10.321 1.00 30.75 B C ATOM 962 N ILE B 47 −5.668 −15.509 5.988 1.00 24.78 B N ATOM 963 CA ILE B 47 −6.883 −14.943 5.405 1.00 22.12 B C ATOM 964 C ILE B 47 −7.777 −16.006 4.768 1.00 25.06 B C ATOM 965 O ILE B 47 −7.330 −16.774 3.914 1.00 26.66 B O ATOM 966 CB ILE B 47 −6.544 −13.927 4.299 1.00 25.90 B C ATOM 967 CG1 ILE B 47 −5.569 −12.864 4.805 1.00 25.54 B C ATOM 968 CG2 ILE B 47 −7.815 −13.286 3.747 1.00 28.25 B C ATOM 969 CD1 ILE B 47 −5.081 −11.952 3.706 1.00 22.33 B C ATOM 970 N PHE B 48 −9.044 −16.035 5.172 1.00 23.95 B N ATOM 971 CA PHE B 48 −10.031 −16.927 4.574 1.00 25.54 B C ATOM 972 C PHE B 48 −11.088 −16.077 3.887 1.00 30.58 B C ATOM 973 O PHE B 48 −11.813 −15.347 4.556 1.00 29.00 B O ATOM 974 CB PHE B 48 −10.725 −17.782 5.646 1.00 25.36 B C ATOM 975 CG PHE B 48 −9.798 −18.674 6.429 1.00 26.77 B C ATOM 976 CD1 PHE B 48 −9.260 −18.251 7.636 1.00 24.64 B C ATOM 977 CD2 PHE B 48 −9.487 −19.946 5.974 1.00 28.62 B C ATOM 978 CE1 PHE B 48 −8.412 −19.074 8.366 1.00 23.95 B C ATOM 979 CE2 PHE B 48 −8.645 −20.775 6.700 1.00 28.73 B C ATOM 980 CZ PHE B 48 −8.107 −20.335 7.898 1.00 25.90 B C ATOM 981 N ASN B 49 −11.197 −16.170 2.565 1.00 23.38 B N ATOM 982 CA ASN B 49 −12.209 −15.384 1.863 1.00 27.57 B C ATOM 983 C ASN B 49 −13.626 −15.824 2.242 1.00 27.92 B C ATOM 984 O ASN B 49 −13.801 −16.750 3.038 1.00 28.71 B O ATOM 985 CB ASN B 49 −11.995 −15.419 0.346 1.00 22.94 B C ATOM 986 CG ASN B 49 −12.275 −16.780 −0.257 1.00 32.75 B C ATOM 987 OD1 ASN B 49 −12.822 −17.671 0.403 1.00 30.86 B O ATOM 988 ND2 ASN B 49 −11.902 −16.949 −1.523 1.00 25.20 B N ATOM 989 N SER B 50 −14.631 −15.158 1.683 1.00 33.24 B N ATOM 990 CA SER B 50 −16.019 −15.449 2.039 1.00 40.75 B C ATOM 991 C SER B 50 −16.472 −16.818 1.540 1.00 40.36 B C ATOM 992 O SER B 50 −17.562 −17.272 1.877 1.00 41.94 B O ATOM 993 CB SER B 50 −16.960 −14.355 1.524 1.00 38.64 B C ATOM 994 OG SER B 50 −16.843 −14.194 0.122 1.00 41.82 B O ATOM 995 N SER B 51 −15.632 −17.468 0.738 1.00 49.72 B N ATOM 996 CA SER B 51 −15.915 −18.819 0.251 1.00 48.33 B C ATOM 997 C SER B 51 −15.090 −19.846 1.015 1.00 48.30 B C ATOM 998 O SER B 51 −14.964 −20.992 0.587 1.00 39.41 B O ATOM 999 CB SER B 51 −15.619 −18.938 −1.247 1.00 44.33 B C ATOM 1000 OG SER B 51 −16.500 −18.134 −2.010 1.00 55.02 B O ATOM 1001 N ASN B 52 −14.514 −19.416 2.135 1.00 47.00 B N ATOM 1002 CA ASN B 52 −13.750 −20.302 3.013 1.00 42.12 B C ATOM 1003 C ASN B 52 −12.414 −20.795 2.464 1.00 41.08 B C ATOM 1004 O ASN B 52 −11.768 −21.645 3.080 1.00 42.93 B O ATOM 1005 CB ASN B 52 −14.604 −21.489 3.462 1.00 49.34 B C ATOM 1006 CG ASN B 52 −15.199 −21.287 4.840 1.00 56.21 B C ATOM 1007 OD1 ASN B 52 −16.408 −21.114 4.993 1.00 46.14 B O ATOM 1008 ND2 ASN B 52 −14.344 −21.299 5.854 1.00 54.50 B N ATOM 1009 N LYS B 53 −11.996 −20.273 1.315 1.00 31.71 B N ATOM 1010 CA LYS B 53 −10.663 −20.590 0.811 1.00 33.29 B C ATOM 1011 C LYS B 53 −9.585 −19.861 1.621 1.00 33.31 B C ATOM 1012 O LYS B 53 −9.771 −18.720 2.044 1.00 27.43 B O ATOM 1013 CB LYS B 53 −10.517 −20.266 −0.679 1.00 27.59 B C ATOM 1014 CG LYS B 53 −9.121 −20.606 −1.208 1.00 36.54 B C ATOM 1015 CD LYS B 53 −9.032 −20.560 −2.730 1.00 42.26 B C ATOM 1016 CE LYS B 53 −7.659 −21.035 −3.201 1.00 35.17 B C ATOM 1017 NZ LYS B 53 −7.479 −20.908 −4.672 1.00 35.78 B N ATOM 1018 N LEU B 54 −8.461 −20.537 1.829 1.00 33.51 B N ATOM 1019 CA LEU B 54 −7.380 −20.017 2.652 1.00 27.32 B C ATOM 1020 C LEU B 54 −6.290 −19.334 1.820 1.00 29.53 B C ATOM 1021 O LEU B 54 −5.893 −19.830 0.767 1.00 36.19 B O ATOM 1022 CB LEU B 54 −6.781 −21.156 3.480 1.00 31.38 B C ATOM 1023 CG LEU B 54 −5.476 −20.910 4.237 1.00 33.67 B C ATOM 1024 CD1 LEU B 54 −5.650 −19.818 5.278 1.00 27.50 B C ATOM 1025 CD2 LEU B 54 −4.986 −22.199 4.882 1.00 32.84 B C ATOM 1026 N PHE B 55 −5.824 −18.185 2.297 1.00 28.75 B N ATOM 1027 CA PHE B 55 −4.682 −17.494 1.708 1.00 27.50 B C ATOM 1028 C PHE B 55 −3.775 −17.062 2.846 1.00 25.87 B C ATOM 1029 O PHE B 55 −4.255 −16.629 3.884 1.00 32.23 B O ATOM 1030 CB PHE B 55 −5.131 −16.261 0.921 1.00 27.64 B C ATOM 1031 CG PHE B 55 −6.026 −16.572 −0.244 1.00 22.94 B C ATOM 1032 CD1 PHE B 55 −7.399 −16.567 −0.096 1.00 22.20 B C ATOM 1033 CD2 PHE B 55 −5.488 −16.854 −1.491 1.00 27.58 B C ATOM 1034 CE1 PHE B 55 −8.226 −16.847 −1.165 1.00 30.38 B C ATOM 1035 CE2 PHE B 55 −6.306 −17.135 −2.572 1.00 26.44 B C ATOM 1036 CZ PHE B 55 −7.681 −17.130 −2.408 1.00 32.90 B C ATOM 1037 N GLN B 56 −2.467 −17.172 2.668 1.00 28.02 B N ATOM 1038 CA GLN B 56 −1.576 −16.878 3.773 1.00 27.44 B C ATOM 1039 C GLN B 56 −0.267 −16.221 3.363 1.00 31.46 B C ATOM 1040 O GLN B 56 0.192 −16.362 2.231 1.00 37.98 B O ATOM 1041 CB GLN B 56 −1.301 −18.151 4.576 1.00 33.26 B C ATOM 1042 CG GLN B 56 −0.939 −19.360 3.730 1.00 32.44 B C ATOM 1043 CD GLN B 56 −0.622 −20.589 4.571 1.00 41.26 B C ATOM 1044 OE1 GLN B 56 0.246 −20.552 5.445 1.00 40.41 B O ATOM 1045 NE2 GLN B 56 −1.325 −21.687 4.305 1.00 39.56 B N ATOM 1046 N TYR B 57 0.317 −15.487 4.302 1.00 21.88 B N ATOM 1047 CA TYR B 57 1.658 −14.946 4.150 1.00 22.42 B C ATOM 1048 C TYR B 57 2.390 −15.047 5.480 1.00 22.08 B C ATOM 1049 O TYR B 57 1.793 −14.877 6.539 1.00 23.51 B O ATOM 1050 CB TYR B 57 1.638 −13.479 3.701 1.00 24.62 B C ATOM 1051 CG TYR B 57 2.957 −12.787 3.985 1.00 23.21 B C ATOM 1052 CD1 TYR B 57 4.037 −12.924 3.120 1.00 24.26 B C ATOM 1053 CD2 TYR B 57 3.137 −12.036 5.140 1.00 21.52 B C ATOM 1054 CE1 TYR B 57 5.252 −12.318 3.387 1.00 22.38 B C ATOM 1055 CE2 TYR B 57 4.348 −11.422 5.416 1.00 20.47 B C ATOM 1056 CZ TYR B 57 5.402 −11.565 4.537 1.00 25.24 B C ATOM 1057 OH TYR B 57 6.609 −10.950 4.805 1.00 20.23 B O ATOM 1058 N ALA B 58 3.689 −15.308 5.424 1.00 21.77 B N ATOM 1059 CA ALA B 58 4.499 −15.335 6.631 1.00 24.55 B C ATOM 1060 C ALA B 58 5.950 −14.993 6.308 1.00 20.16 B C ATOM 1061 O ALA B 58 6.479 −15.431 5.294 1.00 20.99 B O ATOM 1062 CB ALA B 58 4.393 −16.689 7.302 1.00 27.40 B C ATOM 1063 N SER B 59 6.585 −14.199 7.168 1.00 24.98 B N ATOM 1064 CA SER B 59 7.967 −13.781 6.941 1.00 26.54 B C ATOM 1065 C SER B 59 8.948 −14.926 7.182 1.00 30.03 B C ATOM 1066 O SER B 59 10.132 −14.809 6.877 1.00 21.34 B O ATOM 1067 CB SER B 59 8.327 −12.559 7.794 1.00 22.90 B C ATOM 1068 OG SER B 59 8.172 −12.824 9.179 1.00 25.51 B O ATOM 1069 N THR B 60 8.439 −16.020 7.748 1.00 48.65 B N ATOM 1070 CA THR B 60 9.151 −17.296 7.827 1.00 46.35 B C ATOM 1071 C THR B 60 8.101 −18.397 7.770 1.00 52.29 B C ATOM 1072 O THR B 60 6.948 −18.134 7.434 1.00 49.50 B O ATOM 1073 CB THR B 60 9.948 −17.458 9.134 1.00 54.49 B C ATOM 1074 OG1 THR B 60 9.042 −17.536 10.243 1.00 57.06 B O ATOM 1075 CG2 THR B 60 10.910 −16.295 9.340 1.00 65.06 B C ATOM 1076 N ASP B 61 8.486 −19.625 8.104 1.00 37.07 B N ATOM 1077 CA ASP B 61 7.527 −20.726 8.124 1.00 35.62 B C ATOM 1078 C ASP B 61 6.343 −20.347 9.009 1.00 40.19 B C ATOM 1079 O ASP B 61 6.513 −19.998 10.183 1.00 36.11 B O ATOM 1080 CB ASP B 61 8.173 −22.024 8.623 1.00 41.27 B C ATOM 1081 CG ASP B 61 9.378 −22.440 7.792 1.00 49.43 B C ATOM 1082 OD1 ASP B 61 10.392 −21.707 7.787 1.00 53.39 B O ATOM 1083 OD2 ASP B 61 9.320 −23.512 7.156 1.00 44.21 B O ATOM 1084 N MET B 62 5.146 −20.409 8.432 1.00 43.31 B N ATOM 1085 CA MET B 62 3.926 −20.014 9.128 1.00 38.52 B C ATOM 1086 C MET B 62 3.808 −20.643 10.511 1.00 42.96 B C ATOM 1087 O MET B 62 3.315 −20.015 11.451 1.00 41.37 B O ATOM 1088 CB MET B 62 2.696 −20.381 8.301 1.00 31.75 B C ATOM 1089 CG MET B 62 1.390 −20.116 9.027 1.00 37.30 B C ATOM 1090 SD MET B 62 1.265 −18.411 9.606 1.00 31.33 B S ATOM 1091 CE MET B 62 0.980 −17.545 8.070 1.00 24.54 B C ATOM 1092 N ASP B 63 4.265 −21.884 10.629 1.00 49.42 B N ATOM 1093 CA ASP B 63 4.104 −22.643 11.862 1.00 47.63 B C ATOM 1094 C ASP B 63 5.076 −22.198 12.950 1.00 44.15 B C ATOM 1095 O ASP B 63 4.859 −22.462 14.127 1.00 46.49 B O ATOM 1096 CB ASP B 63 4.250 −24.140 11.587 1.00 59.12 B C ATOM 1097 CG ASP B 63 3.201 −24.656 10.616 1.00 66.90 B C ATOM 1098 OD1 ASP B 63 2.006 −24.684 10.985 1.00 59.57 B O ATOM 1099 OD2 ASP B 63 3.576 −25.034 9.483 1.00 67.57 B O ATOM 1100 N LYS B 64 6.147 −21.520 12.558 1.00 41.21 B N ATOM 1101 CA LYS B 64 7.111 −21.032 13.536 1.00 39.98 B C ATOM 1102 C LYS B 64 6.595 −19.774 14.237 1.00 39.97 B C ATOM 1103 O LYS B 64 6.717 −19.639 15.454 1.00 33.04 B O ATOM 1104 CB LYS B 64 8.471 −20.785 12.880 1.00 44.04 B C ATOM 1105 CG LYS B 64 9.091 −22.046 12.290 1.00 54.30 B C ATOM 1106 CD LYS B 64 10.492 −21.798 11.749 1.00 57.87 B C ATOM 1107 CE LYS B 64 11.106 −23.085 11.213 1.00 56.54 B C ATOM 1108 NZ LYS B 64 12.416 −22.845 10.554 1.00 57.68 B N ATOM 1109 N VAL B 65 6.011 −18.862 13.464 1.00 35.84 B N ATOM 1110 CA VAL B 65 5.418 −17.651 14.022 1.00 32.80 B C ATOM 1111 C VAL B 65 4.295 −18.006 14.994 1.00 32.81 B C ATOM 1112 O VAL B 65 4.166 −17.406 16.067 1.00 29.45 B O ATOM 1113 CB VAL B 65 4.836 −16.746 12.919 1.00 30.22 B C ATOM 1114 CG1 VAL B 65 4.343 −15.435 13.517 1.00 25.45 B C ATOM 1115 CG2 VAL B 65 5.868 −16.493 11.835 1.00 34.33 B C ATOM 1116 N LEU B 66 3.488 −18.990 14.610 1.00 29.80 B N ATOM 1117 CA LEU B 66 2.369 −19.424 15.430 1.00 34.20 B C ATOM 1118 C LEU B 66 2.828 −19.990 16.773 1.00 41.26 B C ATOM 1119 O LEU B 66 2.331 −19.586 17.827 1.00 39.01 B O ATOM 1120 CB LEU B 66 1.517 −20.443 14.673 1.00 35.53 B C ATOM 1121 CG LEU B 66 0.792 −19.857 13.460 1.00 36.37 B C ATOM 1122 CD1 LEU B 66 −0.167 −20.870 12.864 1.00 31.71 B C ATOM 1123 CD2 LEU B 66 0.056 −18.584 13.861 1.00 31.61 B C ATOM 1124 N LEU B 67 3.779 −20.917 16.737 1.00 41.41 B N ATOM 1125 CA LEU B 67 4.285 −21.510 17.967 1.00 41.65 B C ATOM 1126 C LEU B 67 4.886 −20.442 18.870 1.00 41.31 B C ATOM 1127 O LEU B 67 4.796 −20.532 20.093 1.00 44.99 B O ATOM 1128 CB LEU B 67 5.309 −22.611 17.672 1.00 44.98 B C ATOM 1129 CG LEU B 67 4.740 −24.028 17.518 1.00 46.47 B C ATOM 1130 CD1 LEU B 67 3.909 −24.399 18.741 1.00 51.36 B C ATOM 1131 CD2 LEU B 67 3.910 −24.170 16.247 1.00 47.13 B C ATOM 1132 N LYS B 68 5.490 −19.429 18.260 1.00 30.15 B N ATOM 1133 CA LYS B 68 6.064 −18.321 19.007 1.00 28.49 B C ATOM 1134 C LYS B 68 4.952 −17.512 19.664 1.00 36.89 B C ATOM 1135 O LYS B 68 5.133 −16.932 20.736 1.00 38.72 B O ATOM 1136 CB LYS B 68 6.905 −17.433 18.087 1.00 31.22 B C ATOM 1137 CG LYS B 68 7.590 −16.276 18.794 1.00 36.27 B C ATOM 1138 CD LYS B 68 8.714 −15.695 17.952 1.00 41.13 B C ATOM 1139 CE LYS B 68 9.450 −14.598 18.705 1.00 38.43 B C ATOM 1140 NZ LYS B 68 10.588 −14.050 17.922 1.00 37.80 B N ATOM 1141 N TYR B 69 3.794 −17.486 19.013 1.00 39.71 B N ATOM 1142 CA TYR B 69 2.631 −16.793 19.547 1.00 41.49 B C ATOM 1143 C TYR B 69 2.057 −17.534 20.750 1.00 40.39 B C ATOM 1144 O TYR B 69 1.821 −16.941 21.803 1.00 39.82 B O ATOM 1145 CB TYR B 69 1.561 −16.645 18.464 1.00 36.39 B C ATOM 1146 CG TYR B 69 0.250 −16.092 18.968 1.00 31.52 B C ATOM 1147 CD1 TYR B 69 0.068 −14.727 19.125 1.00 28.35 B C ATOM 1148 CD2 TYR B 69 −0.805 −16.935 19.284 1.00 32.82 B C ATOM 1149 CE1 TYR B 69 −1.126 −14.217 19.581 1.00 26.39 B C ATOM 1150 CE2 TYR B 69 −2.006 −16.432 19.744 1.00 26.38 B C ATOM 1151 CZ TYR B 69 −2.160 −15.072 19.889 1.00 27.61 B C ATOM 1152 OH TYR B 69 −3.352 −14.558 20.349 1.00 30.19 B O ATOM 1153 N THR B 70 1.828 −18.832 20.586 1.00 34.49 B N ATOM 1154 CA THR B 70 1.244 −19.635 21.652 1.00 40.30 B C ATOM 1155 C THR B 70 2.209 −19.763 22.824 1.00 43.81 B C ATOM 1156 O THR B 70 1.792 −19.786 23.982 1.00 52.58 B O ATOM 1157 CB THR B 70 0.812 −21.030 21.152 1.00 41.92 B C ATOM 1158 OG1 THR B 70 1.903 −21.656 20.466 1.00 51.10 B O ATOM 1159 CG2 THR B 70 −0.368 −20.909 20.198 1.00 38.12 B C ATOM 1160 N GLU B 71 3.501 −19.835 22.521 1.00 44.26 B N ATOM 1161 CA GLU B 71 4.524 −19.856 23.561 1.00 52.17 B C ATOM 1162 C GLU B 71 4.573 −18.509 24.278 1.00 47.45 B C ATOM 1163 O GLU B 71 4.934 −18.430 25.452 1.00 51.35 B O ATOM 1164 CB GLU B 71 5.899 −20.193 22.970 1.00 41.33 B C ATOM 1165 N TYR B 72 4.206 −17.453 23.557 1.00 47.78 B N ATOM 1166 CA TYR B 72 4.186 −16.103 24.107 1.00 49.37 B C ATOM 1167 C TYR B 72 3.136 −16.007 25.205 1.00 57.87 B C ATOM 1168 O TYR B 72 3.440 −15.631 26.340 1.00 57.55 B O ATOM 1169 CB TYR B 72 3.871 −15.097 22.997 1.00 50.17 B C ATOM 1170 CG TYR B 72 4.235 −13.657 23.302 1.00 46.16 B C ATOM 1171 CD1 TYR B 72 5.430 −13.114 22.846 1.00 41.62 B C ATOM 1172 CD2 TYR B 72 3.374 −12.833 24.024 1.00 47.37 B C ATOM 1173 CE1 TYR B 72 5.768 −11.798 23.107 1.00 38.98 B C ATOM 1174 CE2 TYR B 72 3.702 −11.509 24.291 1.00 41.15 B C ATOM 1175 CZ TYR B 72 4.903 −11.000 23.828 1.00 46.34 B C ATOM 1176 OH TYR B 72 5.246 −9.691 24.081 1.00 48.06 B O ATOM 1177 N ASN B 73 1.900 −16.354 24.854 1.00 73.31 B N ATOM 1178 CA ASN B 73 0.776 −16.302 25.784 1.00 74.49 B C ATOM 1179 C ASN B 73 0.903 −17.343 26.894 1.00 82.99 B C ATOM 1180 O ASN B 73 0.162 −18.328 26.926 1.00 80.74 B O ATOM 1181 CB ASN B 73 −0.557 −16.487 25.042 1.00 71.38 B C ATOM 1182 CG ASN B 73 −0.860 −15.349 24.071 1.00 61.49 B C ATOM 1183 OD1 ASN B 73 −1.840 −14.621 24.237 1.00 64.97 B O ATOM 1184 ND2 ASN B 73 −0.023 −15.198 23.053 1.00 53.52 B N TER ATOM 1185 O5′ ADE E 1 −18.730 −9.736 −18.656 1.00 29.47 E O ATOM 1186 C5′ ADE E 1 −18.988 −11.075 −19.073 1.00 30.92 E C ATOM 1187 C4′ ADE E 1 −17.709 −11.792 −19.477 1.00 31.56 E C ATOM 1188 O4′ ADE E 1 −17.094 −11.116 −20.606 1.00 28.61 E O ATOM 1189 C3′ ADE E 1 −16.621 −11.853 −18.406 1.00 35.77 E C ATOM 1190 O3′ ADE E 1 −15.887 −13.057 −18.533 1.00 31.63 E O ATOM 1191 C2′ ADE E 1 −15.739 −10.670 −18.779 1.00 36.34 E C ATOM 1192 C1′ ADE E 1 −15.738 −10.885 −20.284 1.00 30.42 E C ATOM 1193 N9 ADE E 1 −15.256 −9.747 −21.050 1.00 30.35 E N ATOM 1194 C8 ADE E 1 −14.044 −9.644 −21.669 1.00 31.25 E C ATOM 1195 N7 ADE E 1 −13.867 −8.508 −22.293 1.00 29.12 E N ATOM 1196 C5 ADE E 1 −15.041 −7.823 −22.062 1.00 24.57 E C ATOM 1197 C6 ADE E 1 −15.465 −6.552 −22.461 1.00 26.42 E C ATOM 1198 N6 ADE E 1 −14.705 −5.753 −23.207 1.00 29.08 E N ATOM 1199 N1 ADE E 1 −16.693 −6.147 −22.069 1.00 32.94 E N ATOM 1200 C2 ADE E 1 −17.434 −6.980 −21.321 1.00 32.52 E C ATOM 1201 N3 ADE E 1 −17.138 −8.206 −20.882 1.00 29.17 E N ATOM 1202 C4 ADE E 1 −15.913 −8.567 −21.297 1.00 28.60 E C ATOM 1203 P ADE E 2 −14.960 −13.540 −17.328 1.00 39.32 E P ATOM 1204 OP1 ADE E 2 −14.609 −14.955 −17.546 1.00 40.48 E O ATOM 1205 OP2 ADE E 2 −15.600 −13.127 −16.063 1.00 34.58 E O ATOM 1206 O5′ ADE E 2 −13.642 −12.657 −17.522 1.00 46.72 E O ATOM 1207 C5′ ADE E 2 −12.623 −13.009 −18.459 1.00 35.44 E C ATOM 1208 C4′ ADE E 2 −11.485 −12.005 −18.354 1.00 37.56 E C ATOM 1209 O4′ ADE E 2 −11.957 −10.700 −18.795 1.00 40.64 E O ATOM 1210 C3′ ADE E 2 −10.967 −11.762 −16.938 1.00 35.93 E C ATOM 1211 O3′ ADE E 2 −9.635 −11.291 −16.984 1.00 43.80 E O ATOM 1212 C2′ ADE E 2 −11.869 −10.630 −16.474 1.00 37.03 E C ATOM 1213 C1′ ADE E 2 −11.769 −9.786 −17.734 1.00 32.46 E C ATOM 1214 N9 ADE E 2 −12.739 −8.703 −17.801 1.00 30.38 E N ATOM 1215 C8 ADE E 2 −13.795 −8.479 −16.959 1.00 33.19 E C ATOM 1216 N7 ADE E 2 −14.493 −7.404 −17.259 1.00 31.00 E N ATOM 1217 C5 ADE E 2 −13.843 −6.893 −18.372 1.00 30.47 E C ATOM 1218 C6 ADE E 2 −14.084 −5.764 −19.174 1.00 29.69 E C ATOM 1219 N6 ADE E 2 −15.097 −4.919 −18.959 1.00 30.34 E N ATOM 1220 N1 ADE E 2 −13.242 −5.537 −20.202 1.00 27.90 E N ATOM 1221 C2 ADE E 2 −12.230 −6.383 −20.416 1.00 27.22 E C ATOM 1222 N3 ADE E 2 −11.905 −7.479 −19.735 1.00 27.95 E N ATOM 1223 C4 ADE E 2 −12.760 −7.679 −18.718 1.00 29.70 E C ATOM 1224 P ADE E 3 −8.398 −12.239 −16.627 1.00 42.48 E P ATOM 1225 OP1 ADE E 3 −8.627 −13.552 −17.273 1.00 38.14 E O ATOM 1226 OP2 ADE E 3 −8.173 −12.152 −15.165 1.00 39.30 E O ATOM 1227 O5′ ADE E 3 −7.186 −11.486 −17.357 1.00 35.22 E O ATOM 1228 C5′ ADE E 3 −7.251 −11.226 −18.752 1.00 29.83 E C ATOM 1229 C4′ ADE E 3 −6.680 −9.856 −19.079 1.00 33.29 E C ATOM 1230 O4′ ADE E 3 −7.724 −8.849 −19.015 1.00 30.41 E O ATOM 1231 C3′ ADE E 3 −5.559 −9.369 −18.163 1.00 40.46 E C ATOM 1232 O3′ ADE E 3 −4.525 −8.798 −18.955 1.00 37.31 E O ATOM 1233 C2′ ADE E 3 −6.237 −8.316 −17.280 1.00 34.29 E C ATOM 1234 C1′ ADE E 3 −7.283 −7.751 −18.235 1.00 37.00 E C ATOM 1235 N9 ADE E 3 −8.454 −7.181 −17.576 1.00 31.30 E N ATOM 1236 CB ADE E 3 −9.136 −7.698 −16.508 1.00 30.32 E C ATOM 1237 N7 ADE E 3 −10.162 −6.971 −16.133 1.00 31.10 E N ATOM 1238 C5 ADE E 3 −10.153 −5.905 −17.019 1.00 29.56 E C ATOM 1239 C6 ADE E 3 −10.988 −4.779 −17.159 1.00 28.07 E C ATOM 1240 N6 ADE E 3 −12.036 −4.540 −16.363 1.00 32.00 E N ATOM 1241 N1 ADE E 3 −10.700 −3.905 −18.150 1.00 32.19 E N ATOM 1242 C2 ADE E 3 −9.650 −4.146 −18.946 1.00 29.48 E C ATOM 1243 N3 ADE E 3 −8.799 −5.172 −18.911 1.00 29.41 E N ATOM 1244 C4 ADE E 3 −9.108 −6.019 −17.917 1.00 28.05 E C ATOM 1245 P GUA E 4 −3.192 −8.251 −18.255 1.00 44.81 E P ATOM 1246 OP1 GUA E 4 −2.061 −8.508 −19.174 1.00 26.47 E O ATOM 1247 OP2 GUA E 4 −3.173 −8.771 −16.867 1.00 42.97 E O ATOM 1248 O5′ GUA E 4 −3.445 −6.670 −18.204 1.00 41.54 E O ATOM 1249 C5′ GUA E 4 −3.525 −5.970 −19.443 1.00 41.38 E C ATOM 1250 C4′ GUA E 4 −4.139 −4.590 −19.282 1.00 40.49 E C ATOM 1251 O4′ GUA E 4 −5.362 −4.659 −18.507 1.00 41.29 E O ATOM 1252 C3′ GUA E 4 −3.273 −3.548 −18.579 1.00 49.70 E C ATOM 1253 O3′ GUA E 4 −3.057 −2.496 −19.513 1.00 51.54 E O ATOM 1254 C2′ GUA E 4 −4.099 −3.111 −17.362 1.00 40.72 E C ATOM 1255 C1′ GUA E 4 −5.513 −3.432 −17.833 1.00 35.99 E C ATOM 1256 N9 GUA E 4 −6.536 −3.626 −16.805 1.00 35.36 E N ATOM 1257 C8 GUA E 4 −6.606 −4.633 −15.869 1.00 31.20 E C ATOM 1258 N7 GUA E 4 −7.657 −4.550 −15.094 1.00 30.27 E N ATOM 1259 C5 GUA E 4 −8.334 −3.418 −15.544 1.00 31.07 E C ATOM 1260 C6 GUA E 4 −9.545 −2.824 −15.091 1.00 29.65 E C ATOM 1261 O6 GUA E 4 −10.299 −3.183 −14.166 1.00 25.90 E O ATOM 1262 N1 GUA E 4 −9.863 −1.693 −15.837 1.00 27.69 E N ATOM 1263 C2 GUA E 4 −9.114 −1.197 −16.878 1.00 32.22 E C ATOM 1264 N2 GUA E 4 −9.586 −0.090 −17.471 1.00 36.73 E N ATOM 1265 N3 GUA E 4 −7.981 −1.739 −17.312 1.00 30.68 E N ATOM 1266 C4 GUA E 4 −7.655 −2.844 −16.601 1.00 32.71 E C ATOM 1267 P CYT E 5 −2.178 −1.210 −19.151 1.00 55.63 E P ATOM 1268 OP1 CYT E 5 −1.471 −0.815 −20.393 1.00 38.22 E O ATOM 1269 OP2 CYT E 5 −1.446 −1.473 −17.889 1.00 40.16 E O ATOM 1270 O5′ CYT E 5 −3.303 −0.112 −18.855 1.00 37.38 E O ATOM 1271 C5′ CYT E 5 −4.265 0.131 −19.866 1.00 33.01 E C ATOM 1272 C4′ CYT E 5 −5.032 1.402 −19.579 1.00 33.11 E C ATOM 1273 O4′ CYT E 5 −6.050 1.157 −18.576 1.00 30.77 E O ATOM 1274 C3′ CYT E 5 −4.180 2.557 −19.075 1.00 34.24 E C ATOM 1275 O3′ CYT E 5 −4.639 3.713 −19.760 1.00 39.20 E O ATOM 1276 C2′ CYT E 5 −4.446 2.561 −17.565 1.00 31.20 E C ATOM 1277 C1′ CYT E 5 −5.863 2.000 −17.463 1.00 28.63 E C ATOM 1278 N1 CYT E 5 −6.146 1.145 −16.274 1.00 29.46 E N ATOM 1279 C2 CYT E 5 −7.212 1.483 −15.439 1.00 26.08 E C ATOM 1280 O2 CYT E 5 −7.885 2.490 −15.698 1.00 28.38 E O ATOM 1281 N3 CYT E 5 −7.479 0.700 −14.367 1.00 26.72 E N ATOM 1282 C4 CYT E 5 −6.735 −0.378 −14.115 1.00 25.28 E C ATOM 1283 N4 CYT E 5 −7.053 −1.106 −13.036 1.00 22.58 E N ATOM 1284 C5 CYT E 5 −5.642 −0.745 −14.956 1.00 25.38 E C ATOM 1285 C6 CYT E 5 −5.390 0.038 −16.014 1.00 30.65 E C ATOM 1286 P THY E 6 −4.170 5.191 −19.383 1.00 60.37 E P ATOM 1287 OP1 THY E 6 −4.538 6.060 −20.525 1.00 54.22 E O ATOM 1288 OP2 THY E 6 −2.773 5.142 −18.892 1.00 49.93 E O ATOM 1289 O5′ THY E 6 −5.109 5.566 −18.140 1.00 47.68 E O ATOM 1290 C5′ THY E 6 −6.386 6.162 −18.345 1.00 46.46 E C ATOM 1291 C4′ THY E 6 −6.806 6.961 −17.125 1.00 38.37 E C ATOM 1292 O4′ THY E 6 −7.109 6.050 −16.035 1.00 39.69 E O ATOM 1293 C3′ THY E 6 −5.735 7.892 −16.572 1.00 43.33 E C ATOM 1294 O3′ THY E 6 −6.340 8.950 −15.857 1.00 49.28 E O ATOM 1295 C2′ THY E 6 −5.027 6.982 −15.582 1.00 39.84 E C ATOM 1296 C1′ THY E 6 −6.267 6.372 −14.942 1.00 44.31 E C ATOM 1297 N1 THY E 6 −5.997 5.155 −14.132 1.00 36.55 E N ATOM 1298 C2 THY E 6 −6.920 4.771 −13.188 1.00 34.38 E C ATOM 1299 O2 THY E 6 −7.955 5.381 −12.988 1.00 33.38 E O ATOM 1300 N3 THY E 6 −6.584 3.638 −12.489 1.00 29.23 E N ATOM 1301 C4 THY E 6 −5.440 2.878 −12.640 1.00 30.85 E C ATOM 1302 O4 THY E 6 −5.220 1.878 −11.967 1.00 34.06 E O ATOM 1303 C5 THY E 6 −4.515 3.343 −13.642 1.00 32.80 E C ATOM 1304 C7 THY E 6 −3.238 2.592 −13.883 1.00 27.26 E C ATOM 1305 C6 THY E 6 −4.831 4.446 −14.332 1.00 30.87 E C ATOM 1306 P ADE E 7 −6.618 10.359 −16.554 1.00 45.58 E P ATOM 1307 OP1 ADE E 7 −7.118 10.099 −17.923 1.00 48.75 E O ATOM 1308 OP2 ADE E 7 −5.421 11.205 −16.345 1.00 50.29 E O ATOM 1309 O5′ ADE E 7 −7.804 10.955 −15.662 1.00 37.42 E O ATOM 1310 C5′ ADE E 7 −9.051 10.284 −15.612 1.00 40.53 E C ATOM 1311 C4′ ADE E 7 −9.601 10.242 −14.196 1.00 40.88 E C ATOM 1312 O4′ ADE E 7 −8.962 9.183 −13.434 1.00 42.29 E O ATOM 1313 C3′ ADE E 7 −9.423 11.515 −13.380 1.00 43.86 E C ATOM 1314 O3′ ADE E 7 −10.618 11.704 −12.623 1.00 46.18 E O ATOM 1315 C2′ ADE E 7 −8.191 11.211 −12.518 1.00 38.63 E C ATOM 1316 C1′ ADE E 7 −8.329 9.708 −12.280 1.00 40.37 E C ATOM 1317 N9 ADE E 7 −7.083 8.955 −12.110 1.00 35.39 E N ATOM 1318 C8 ADE E 7 −5.878 9.165 −12.724 1.00 38.43 E C ATOM 1319 N7 ADE E 7 −4.946 8.303 −12.375 1.00 38.83 E N ATOM 1320 C5 ADE E 7 −5.583 7.461 −11.475 1.00 32.45 E C ATOM 1321 C6 ADE E 7 −5.153 6.335 −10.738 1.00 28.45 E C ATOM 1322 N6 ADE E 7 −3.917 5.831 −10.788 1.00 23.96 E N ATOM 1323 N1 ADE E 7 −6.052 5.733 −9.930 1.00 28.10 E N ATOM 1324 C2 ADE E 7 −7.293 6.222 −9.866 1.00 28.25 E C ATOM 1325 N3 ADE E 7 −7.814 7.266 −10.509 1.00 34.76 E N ATOM 1326 C4 ADE E 7 −6.901 7.849 −11.306 1.00 35.01 E C ATOM 1327 P THY E 8 −10.849 13.012 −11.730 1.00 56.64 E P ATOM 1328 OP1 THY E 8 −12.282 13.371 −11.831 1.00 50.90 E O ATOM 1329 OP2 THY E 8 −9.782 13.995 −12.048 1.00 41.51 E O ATOM 1330 O5′ THY E 8 −10.591 12.465 −10.254 1.00 37.60 E O ATOM 1331 C5′ THY E 8 −11.256 11.287 −9.857 1.00 37.93 E C ATOM 1332 C4′ THY E 8 −10.552 10.694 −8.657 1.00 38.57 E C ATOM 1333 O4′ THY E 8 −9.292 10.106 −9.047 1.00 40.12 E O ATOM 1334 C3′ THY E 8 −10.174 11.692 −7.570 1.00 30.77 E C ATOM 1335 O3′ THY E 8 −11.212 11.693 −6.602 1.00 31.18 E O ATOM 1336 C2′ THY E 8 −8.839 11.161 −7.031 1.00 28.75 E C ATOM 1337 C1′ THY E 8 −8.637 9.870 −7.823 1.00 31.57 E C ATOM 1338 N1 THY E 8 −7.211 9.446 −8.069 1.00 30.96 E N ATOM 1339 C2 THY E 8 −6.738 8.325 −7.418 1.00 29.46 E C ATOM 1340 O2 THY E 8 −7.411 7.658 −6.647 1.00 28.41 E O ATOM 1341 N3 THY E 8 −5.434 8.008 −7.696 1.00 25.51 E N ATOM 1342 C4 THY E 8 −4.573 8.678 −8.543 1.00 28.41 E C ATOM 1343 O4 THY E 8 −3.414 8.304 −8.725 1.00 24.27 E O ATOM 1344 C5 THY E 8 −5.133 9.838 −9.195 1.00 28.63 E C ATOM 1345 C7 THY E 8 −4.291 10.650 −10.138 1.00 36.79 E C ATOM 1346 C6 THY E 8 −6.405 10.163 −8.930 1.00 26.96 E C ATOM 1347 P THY E 9 −11.056 12.419 −5.183 1.00 42.41 E P ATOM 1348 OP1 THY E 9 −12.415 12.694 −4.663 1.00 31.14 E O ATOM 1349 OP2 THY E 9 −10.054 13.502 −5.314 1.00 35.31 E O ATOM 1350 O5′ THY E 9 −10.434 11.264 −4.279 1.00 37.55 E O ATOM 1351 C5′ THY E 9 −11.266 10.160 −3.990 1.00 35.57 E C ATOM 1352 C4′ THY E 9 −10.478 9.121 −3.227 1.00 33.83 E C ATOM 1353 O4′ THY E 9 −9.220 8.899 −3.906 1.00 29.86 E O ATOM 1354 C3′ THY E 9 −10.144 9.494 −1.786 1.00 28.03 E C ATOM 1355 O3′ THY E 9 −10.370 8.323 −1.022 1.00 31.20 E O ATOM 1356 C2′ THY E 9 −8.675 9.907 −1.859 1.00 27.45 E C ATOM 1357 C1′ THY E 9 −8.172 8.985 −2.967 1.00 31.01 E C ATOM 1358 N1 THY E 9 −6.962 9.450 −3.704 1.00 28.12 E N ATOM 1359 C2 THY E 9 −5.909 8.582 −3.811 1.00 25.18 E C ATOM 1360 O2 THY E 9 −5.927 7.464 −3.328 1.00 26.89 E O ATOM 1361 N3 THY E 9 −4.838 9.074 −4.507 1.00 26.79 E N ATOM 1362 C4 THY E 9 −4.717 10.316 −5.095 1.00 24.43 E C ATOM 1363 O4 THY E 9 −3.708 10.664 −5.700 1.00 27.08 E O ATOM 1364 C5 THY E 9 −5.853 11.178 −4.945 1.00 26.20 E C ATOM 1365 C7 THY E 9 −5.819 12.553 −5.545 1.00 26.68 E C ATOM 1366 C6 THY E 9 −6.911 10.711 −4.266 1.00 30.99 E C ATOM 1367 P ADE E 10 −10.116 8.233 0.551 1.00 27.69 E P ATOM 1368 OP1 ADE E 10 −10.999 7.180 1.102 1.00 25.31 E O ATOM 1369 OP2 ADE E 10 −10.161 9.594 1.123 1.00 31.49 E O ATOM 1370 O5′ ADE E 10 −8.616 7.674 0.595 1.00 37.35 E O ATOM 1371 C5′ ADE E 10 −8.361 6.335 0.171 1.00 23.82 E C ATOM 1372 C4′ ADE E 10 −6.969 5.856 0.564 1.00 22.72 E C ATOM 1373 O4′ ADE E 10 −5.977 6.502 −0.266 1.00 23.11 E O ATOM 1374 C3′ ADE E 10 −6.531 6.128 2.002 1.00 25.58 E C ATOM 1375 O3′ ADE E 10 −5.853 4.975 2.479 1.00 22.92 E O ATOM 1376 C2′ ADE E 10 −5.596 7.330 1.881 1.00 19.12 E C ATOM 1377 C1′ ADE E 10 −4.945 7.047 0.533 1.00 23.66 E C ATOM 1378 N9 ADE E 10 −4.450 8.219 −0.185 1.00 23.63 E N ATOM 1379 C8 ADE E 10 −5.137 9.377 −0.427 1.00 20.43 E C ATOM 1380 N7 ADE E 10 −4.449 10.259 −1.116 1.00 21.56 E N ATOM 1381 C5 ADE E 10 −3.232 9.637 −1.348 1.00 20.27 E C ATOM 1382 C6 ADE E 10 −2.065 10.050 −2.026 1.00 23.27 E C ATOM 1383 N6 ADE E 10 −1.935 11.243 −2.621 1.00 22.55 E N ATOM 1384 N1 ADE E 10 −1.028 9.186 −2.072 1.00 21.68 E N ATOM 1385 C2 ADE E 10 −1.159 7.995 −1.473 1.00 20.08 E C ATOM 1386 N3 ADE E 10 −2.204 7.498 −0.811 1.00 21.84 E N ATOM 1387 C4 ADE E 10 −3.218 8.376 −0.783 1.00 20.33 E C ATOM 1388 P THY E 11 −5.251 4.906 3.959 1.00 30.15 E P ATOM 1389 OP1 THY E 11 −5.489 3.533 4.453 1.00 30.86 E O ATOM 1390 OP2 THY E 11 −5.725 6.061 4.753 1.00 22.38 E O ATOM 1391 O5′ THY E 11 −3.686 5.080 3.667 1.00 31.02 E O ATOM 1392 C5′ THY E 11 −3.054 4.141 2.808 1.00 24.15 E C ATOM 1393 C4′ THY E 11 −1.576 4.434 2.624 1.00 27.89 E C ATOM 1394 O4′ THY E 11 −1.390 5.685 1.914 1.00 25.80 E O ATOM 1395 C3′ THY E 11 −0.762 4.531 3.910 1.00 29.91 E C ATOM 1396 O3′ THY E 11 0.381 3.686 3.729 1.00 26.16 E O ATOM 1397 C2′ THY E 11 −0.441 6.029 4.018 1.00 26.53 E C ATOM 1398 C1′ THY E 11 −0.387 6.444 2.547 1.00 25.90 E C ATOM 1399 N1 THY E 11 −0.686 7.873 2.192 1.00 23.31 E N ATOM 1400 C2 THY E 11 0.223 8.558 1.409 1.00 24.11 E C ATOM 1401 O2 THY E 11 1.270 8.088 1.011 1.00 29.11 E O ATOM 1402 N3 THY E 11 −0.121 9.841 1.100 1.00 22.87 E N ATOM 1403 C4 THY E 11 −1.265 10.498 1.485 1.00 28.65 E C ATOM 1404 O4 THY E 11 −1.474 11.662 1.151 1.00 36.71 E O ATOM 1405 C5 THY E 11 −2.185 9.732 2.295 1.00 24.77 E C ATOM 1406 C7 THY E 11 −3.464 10.372 2.759 1.00 24.15 E C ATOM 1407 C6 THY E 11 −1.862 8.466 2.606 1.00 22.01 E C ATOM 1408 P THY E 12 1.421 3.356 4.904 1.00 25.44 E P ATOM 1409 OP1 THY E 12 2.065 2.075 4.536 1.00 24.55 E O ATOM 1410 OP2 THY E 12 0.765 3.505 6.222 1.00 32.62 E O ATOM 1411 O5′ THY E 12 2.496 4.537 4.755 1.00 26.81 E O ATOM 1412 C5′ THY E 12 3.296 4.563 3.566 1.00 21.48 E C ATOM 1413 C4′ THY E 12 4.129 5.825 3.493 1.00 23.82 E C ATOM 1414 O4′ THY E 12 3.290 6.969 3.188 1.00 23.67 E O ATOM 1415 C3′ THY E 12 4.867 6.182 4.783 1.00 24.81 E C ATOM 1416 O3′ THY E 12 6.206 6.506 4.466 1.00 25.36 E O ATOM 1417 C2′ THY E 12 4.120 7.416 5.290 1.00 18.68 E C ATOM 1418 C1′ THY E 12 3.788 8.050 3.948 1.00 20.51 E C ATOM 1419 N1 THY E 12 2.771 9.121 3.988 1.00 21.40 E N ATOM 1420 C2 THY E 12 2.955 10.241 3.198 1.00 22.05 E C ATOM 1421 O2 THY E 12 3.910 10.394 2.460 1.00 21.47 E O ATOM 1422 N3 THY E 12 1.967 11.186 3.304 1.00 18.78 E N ATOM 1423 C4 THY E 12 0.843 11.109 4.096 1.00 19.13 E C ATOM 1424 O4 THY E 12 0.012 12.009 4.111 1.00 26.75 E O ATOM 1425 C5 THY E 12 0.713 9.915 4.898 1.00 18.25 E C ATOM 1426 C7 THY E 12 −0.472 9.735 5.805 1.00 19.51 E C ATOM 1427 C6 THY E 12 1.670 8.989 4.811 1.00 19.46 E C ATOM 1428 P ADE E 13 7.377 5.414 4.483 1.00 30.98 E P ATOM 1429 OP1 ADE E 13 7.071 4.389 3.460 1.00 28.50 E O ATOM 1430 OP2 ADE E 13 7.606 5.022 5.896 1.00 23.43 E O ATOM 1431 O5′ ADE E 13 8.623 6.284 3.975 1.00 29.72 E O ATOM 1432 C5′ ADE E 13 8.538 6.922 2.706 1.00 26.78 E C ATOM 1433 C4′ ADE E 13 9.483 8.111 2.612 1.00 31.36 E C ATOM 1434 O4′ ADE E 13 8.780 9.358 2.850 1.00 26.91 E O ATOM 1435 C3′ ADE E 13 10.671 8.113 3.567 1.00 24.84 E C ATOM 1436 O3′ ADE E 13 11.755 8.715 2.871 1.00 25.02 E O ATOM 1437 C2′ ADE E 13 10.168 8.953 4.739 1.00 24.93 E C ATOM 1438 C1′ ADE E 13 9.149 9.897 4.101 1.00 28.31 E C ATOM 1439 N9 ADE E 13 7.913 10.036 4.860 1.00 22.96 E N ATOM 1440 C8 ADE E 13 7.461 9.213 5.849 1.00 20.48 E C ATOM 1441 N7 ADE E 13 6.310 9.588 6.352 1.00 21.80 E N ATOM 1442 C5 ADE E 13 5.977 10.724 5.631 1.00 19.63 E C ATOM 1443 C6 ADE E 13 4.867 11.590 5.680 1.00 20.30 E C ATOM 1444 N6 ADE E 13 3.845 11.428 6.529 1.00 19.00 E N ATOM 1445 N1 ADE E 13 4.852 12.631 4.819 1.00 21.87 E N ATOM 1446 C2 ADE E 13 5.879 12.785 3.971 1.00 21.40 E C ATOM 1447 N3 ADE E 13 6.973 12.039 3.838 1.00 20.80 E N ATOM 1448 C4 ADE E 13 6.958 11.014 4.703 1.00 21.32 E C ATOM 1449 P GUA E 14 13.159 9.030 3.570 1.00 31.66 E P ATOM 1450 OP1 GUA E 14 14.216 8.918 2.535 1.00 31.34 E O ATOM 1451 OP2 GUA E 14 13.251 8.231 4.813 1.00 22.94 E O ATOM 1452 O5′ GUA E 14 13.004 10.579 3.943 1.00 25.42 E O ATOM 1453 C5′ GUA E 14 12.824 11.512 2.891 1.00 25.99 E C ATOM 1454 C4′ GUA E 14 12.492 12.896 3.415 1.00 34.31 E C ATOM 1455 O4′ GUA E 14 11.188 12.895 4.055 1.00 34.27 E O ATOM 1456 C3′ GUA E 14 13.485 13.460 4.429 1.00 37.50 E C ATOM 1457 O3′ GUA E 14 13.899 14.742 3.973 1.00 41.76 E O ATOM 1458 C2′ GUA E 14 12.698 13.526 5.738 1.00 34.47 E C ATOM 1459 C1′ GUA E 14 11.253 13.627 5.258 1.00 31.30 E C ATOM 1460 N9 GUA E 14 10.291 13.055 6.194 1.00 29.91 E N ATOM 1461 C8 GUA E 14 10.424 11.900 6.934 1.00 30.46 E C ATOM 1462 N7 GUA E 14 9.388 11.644 7.689 1.00 28.53 E N ATOM 1463 C5 GUA E 14 8.513 12.695 7.432 1.00 24.42 E C ATOM 1464 C6 GUA E 14 7.230 12.965 7.955 1.00 24.43 E C ATOM 1465 O6 GUA E 14 6.586 12.305 8.777 1.00 28.12 E O ATOM 1466 N1 GUA E 14 6.687 14.137 7.435 1.00 24.65 E N ATOM 1467 C2 GUA E 14 7.309 14.949 6.517 1.00 28.51 E C ATOM 1468 N2 GUA E 14 6.629 16.039 6.125 1.00 28.83 E N ATOM 1469 N3 GUA E 14 8.513 14.708 6.013 1.00 30.78 E N ATOM 1470 C4 GUA E 14 9.053 13.570 6.515 1.00 29.53 E C ATOM 1471 P CYT E 15 14.736 15.739 4.898 1.00 56.84 E P ATOM 1472 OP1 CYT E 15 15.666 16.475 4.014 1.00 65.29 E O ATOM 1473 OP2 CYT E 15 15.262 14.989 6.062 1.00 49.85 E O ATOM 1474 O5′ CYT E 15 13.603 16.748 5.406 1.00 55.19 E O ATOM 1475 C5′ CYT E 15 12.708 17.324 4.454 1.00 56.18 E C ATOM 1476 C4′ CYT E 15 11.642 18.176 5.128 1.00 61.42 E C ATOM 1477 O4′ CYT E 15 10.704 17.348 5.868 1.00 54.03 E O ATOM 1478 C3′ CYT E 15 12.169 19.200 6.129 1.00 63.66 E C ATOM 1479 O3′ CYT E 15 11.386 20.389 6.042 1.00 69.99 E O ATOM 1480 C2′ CYT E 15 11.981 18.488 7.465 1.00 52.85 E C ATOM 1481 C1′ CYT E 15 10.653 17.784 7.212 1.00 49.35 E C ATOM 1482 N1 CYT E 15 10.426 16.603 8.090 1.00 42.67 E N ATOM 1483 C2 CYT E 15 9.266 16.548 8.872 1.00 37.19 E C ATOM 1484 O2 CYT E 15 8.458 17.484 8.812 1.00 38.83 E O ATOM 1485 N3 CYT E 15 9.062 15.470 9.671 1.00 31.91 E N ATOM 1486 C4 CYT E 15 9.963 14.484 9.704 1.00 35.66 E C ATOM 1487 N4 CYT E 15 9.715 13.443 10.508 1.00 33.17 E N ATOM 1488 C5 CYT E 15 11.156 14.526 8.915 1.00 37.46 E C ATOM 1489 C6 CYT E 15 11.346 15.593 8.129 1.00 38.60 E C ATOM 1490 P THY E 16 11.995 21.808 6.469 1.00 78.44 E P ATOM 1491 OP1 THY E 16 11.959 22.665 5.264 1.00 50.40 E O ATOM 1492 OP2 THY E 16 13.261 21.586 7.212 1.00 63.19 E O ATOM 1493 O5′ THY E 16 10.923 22.349 7.524 1.00 70.06 E O ATOM 1494 C5′ THY E 16 9.533 22.263 7.241 1.00 65.61 E C ATOM 1495 C4′ THY E 16 8.750 22.391 8.533 1.00 64.41 E C ATOM 1496 O4′ THY E 16 8.692 21.120 9.230 1.00 56.65 E O ATOM 1497 C3′ THY E 16 9.346 23.382 9.527 1.00 64.90 E C ATOM 1498 O3′ THY E 16 8.281 24.127 10.092 1.00 70.01 E O ATOM 1499 C2′ THY E 16 10.035 22.482 10.552 1.00 55.44 E C ATOM 1500 C1′ THY E 16 9.040 21.330 10.583 1.00 49.98 E C ATOM 1501 N1 THY E 16 9.550 20.043 11.132 1.00 46.89 E N ATOM 1502 C2 THY E 16 8.698 19.308 11.926 1.00 41.72 E C ATOM 1503 O2 THY E 16 7.565 19.677 12.194 1.00 36.25 E O ATOM 1504 N3 THY E 16 9.225 18.128 12.392 1.00 36.45 E N ATOM 1505 C4 THY E 16 10.491 17.628 12.146 1.00 38.15 E C ATOM 1506 O4 THY E 16 10.882 16.559 12.606 1.00 36.21 E O ATOM 1507 C5 THY E 16 11.327 18.448 11.309 1.00 39.53 E C ATOM 1508 C7 THY E 16 12.717 17.982 10.988 1.00 36.66 E C ATOM 1509 C6 THY E 16 10.828 19.603 10.843 1.00 43.44 E C ATOM 1510 P THY E 17 8.549 25.581 10.689 1.00 78.30 E P ATOM 1511 OP1 THY E 17 7.626 26.522 10.012 1.00 60.38 E O ATOM 1512 OP2 THY E 17 10.012 25.813 10.672 1.00 73.87 E O ATOM 1513 O5′ THY E 17 8.116 25.415 12.218 1.00 73.56 E O ATOM 1514 C5′ THY E 17 6.754 25.202 12.576 1.00 68.05 E C ATOM 1515 C4′ THY E 17 6.683 24.775 14.030 1.00 68.97 E C ATOM 1516 O4′ THY E 17 7.266 23.452 14.157 1.00 64.24 E O ATOM 1517 C3′ THY E 17 7.449 25.680 14.994 1.00 65.70 E C ATOM 1518 O3′ THY E 17 6.707 25.874 16.192 1.00 71.08 E O ATOM 1519 C2′ THY E 17 8.741 24.910 15.254 1.00 65.84 E C ATOM 1520 C1′ THY E 17 8.250 23.470 15.169 1.00 71.79 E C ATOM 1521 N1 THY E 17 9.320 22.512 14.802 1.00 62.90 E N ATOM 1522 C2 THY E 17 9.211 21.191 15.192 1.00 55.41 E C ATOM 1523 O2 THY E 17 8.264 20.754 15.830 1.00 43.12 E O ATOM 1524 N3 THY E 17 10.263 20.397 14.798 1.00 44.40 E N ATOM 1525 C4 THY E 17 11.380 20.789 14.081 1.00 46.62 E C ATOM 1526 O4 THY E 17 12.273 20.005 13.779 1.00 49.59 E O ATOM 1527 C5 THY E 17 11.425 22.183 13.711 1.00 62.54 E C ATOM 1528 C7 THY E 17 12.591 22.718 12.930 1.00 69.77 E C ATOM 1529 C6 THY E 17 10.407 22.970 14.086 1.00 59.82 E C TER ATOM 1530 O5′ THY F 1 15.151 15.405 19.847 1.00 35.44 F O ATOM 1531 C5′ THY F 1 15.320 14.944 21.178 1.00 28.60 F C ATOM 1532 C4′ THY F 1 13.978 14.889 21.887 1.00 27.43 F C ATOM 1533 O4′ THY F 1 13.339 16.188 21.818 1.00 29.22 F O ATOM 1534 C3′ THY F 1 12.977 13.892 21.316 1.00 28.97 F C ATOM 1535 O3′ THY F 1 12.248 13.304 22.386 1.00 29.78 F O ATOM 1536 C2′ THY F 1 12.095 14.750 20.407 1.00 32.74 F C ATOM 1537 C1′ THY F 1 12.142 16.129 21.065 1.00 29.02 F C ATOM 1538 N1 THY F 1 12.145 17.296 20.117 1.00 27.55 F N ATOM 1539 C2 THY F 1 11.029 18.102 20.029 1.00 26.62 F C ATOM 1540 O2 THY F 1 10.018 17.923 20.677 1.00 32.29 F O ATOM 1541 N3 THY F 1 11.126 19.142 19.148 1.00 24.47 F N ATOM 1542 C4 THY F 1 12.206 19.455 18.356 1.00 27.28 F C ATOM 1543 O4 THY F 1 12.186 20.415 17.595 1.00 32.91 F O ATOM 1544 C5 THY F 1 13.344 18.577 18.487 1.00 26.29 F C ATOM 1545 C7 THY F 1 14.575 18.823 17.668 1.00 33.04 F C ATOM 1546 C6 THY F 1 13.265 17.553 19.348 1.00 27.16 F C ATOM 1547 P ADE F 2 11.449 11.931 22.178 1.00 39.94 F P ATOM 1548 OP1 ADE F 2 11.319 11.249 23.481 1.00 40.24 F O ATOM 1549 OP2 ADE F 2 12.049 11.216 21.034 1.00 31.49 F O ATOM 1550 O5′ ADE F 2 10.007 12.422 21.708 1.00 39.09 F O ATOM 1551 C5′ ADE F 2 9.242 13.377 22.427 1.00 26.83 F C ATOM 1552 C4′ ADE F 2 8.068 13.787 21.551 1.00 33.76 F C ATOM 1553 O4′ ADE F 2 8.510 14.720 20.526 1.00 38.96 F O ATOM 1554 C3′ ADE F 2 7.419 12.650 20.766 1.00 35.68 F C ATOM 1555 O3′ ADE F 2 6.097 13.018 20.473 1.00 42.23 F O ATOM 1556 C2′ ADE F 2 8.221 12.663 19.471 1.00 30.26 F C ATOM 1557 C1′ ADE F 2 8.209 14.169 19.255 1.00 30.49 F C ATOM 1558 N9 ADE F 2 9.163 14.657 18.268 1.00 26.53 F N ATOM 1559 C8 ADE F 2 10.195 13.977 17.681 1.00 28.86 F C ATOM 1560 N7 ADE F 2 10.879 14.698 16.815 1.00 28.94 F N ATOM 1561 C5 ADE F 2 10.251 15.934 16.841 1.00 27.05 F C ATOM 1562 C6 ADE F 2 10.482 17.144 16.157 1.00 25.84 F C ATOM 1563 N6 ADE F 2 11.464 17.322 15.272 1.00 28.80 F N ATOM 1564 N1 ADE F 2 9.662 18.179 16.421 1.00 25.80 F N ATOM 1565 C2 ADE F 2 8.678 18.020 17.310 1.00 24.88 F C ATOM 1566 N3 ADE F 2 8.363 16.936 18.012 1.00 26.79 F N ATOM 1567 C4 ADE F 2 9.192 15.922 17.731 1.00 27.44 F C ATOM 1568 P ADE F 3 4.853 12.162 20.988 1.00 39.47 F P ATOM 1569 OP1 ADE F 3 4.873 12.164 22.468 1.00 40.90 F O ATOM 1570 OP2 ADE F 3 4.808 10.885 20.235 1.00 38.47 F O ATOM 1571 O5′ ADE F 3 3.662 13.097 20.486 1.00 32.45 F O ATOM 1572 C5′ ADE F 3 3.672 14.458 20.891 1.00 32.40 F C ATOM 1573 C4′ ADE F 3 3.160 15.342 19.773 1.00 28.86 F C ATOM 1574 O4′ ADE F 3 4.231 15.629 18.842 1.00 28.94 F O ATOM 1575 C3′ ADE F 3 2.036 14.721 18.953 1.00 39.96 F C ATOM 1576 O3′ ADE F 3 0.991 15.679 18.813 1.00 36.97 F O ATOM 1577 C2′ ADE F 3 2.694 14.359 17.614 1.00 33.14 F C ATOM 1578 C1′ ADE F 3 3.792 15.414 17.514 1.00 36.24 F C ATOM 1579 N9 ADE F 3 4.967 15.021 16.739 1.00 28.30 F N ATOM 1580 C8 ADE F 3 5.621 13.819 16.767 1.00 29.94 F C ATOM 1581 N7 ADE F 3 6.663 13.762 15.969 1.00 29.86 F N ATOM 1582 C5 ADE F 3 6.697 15.018 15.379 1.00 29.66 F C ATOM 1583 C6 ADE F 3 7.562 15.605 14.433 1.00 26.28 F C ATOM 1584 N6 ADE F 3 8.605 14.972 13.892 1.00 30.60 F N ATOM 1585 N1 ADE F 3 7.314 16.879 14.061 1.00 28.86 F N ATOM 1586 C2 ADE F 3 6.267 17.520 14.600 1.00 28.38 F C ATOM 1587 N3 ADE F 3 5.387 17.076 15.499 1.00 30.45 F N ATOM 1588 C4 ADE F 3 5.660 15.807 15.848 1.00 30.12 F C ATOM 1589 P GUA F 4 −0.306 15.279 17.977 1.00 36.44 F P ATOM 1590 OP1 GUA F 4 −1.461 15.980 18.572 1.00 30.12 F O ATOM 1591 OP2 GUA F 4 −0.313 13.800 17.840 1.00 37.68 F O ATOM 1592 O5′ GUA F 4 0.019 15.913 16.539 1.00 38.14 F O ATOM 1593 C5′ GUA F 4 0.319 17.304 16.457 1.00 34.43 F C ATOM 1594 C4′ GUA F 4 0.845 17.689 15.083 1.00 37.40 F C ATOM 1595 O4′ GUA F 4 2.082 16.992 14.785 1.00 40.03 F O ATOM 1596 C3′ GUA F 4 −0.082 17.399 13.905 1.00 48.37 F C ATOM 1597 O3′ GUA F 4 −0.224 18.621 13.194 1.00 50.22 F O ATOM 1598 C2′ GUA F 4 0.650 16.322 13.096 1.00 37.79 F C ATOM 1599 C1′ GUA F 4 2.096 16.693 13.404 1.00 35.99 F C ATOM 1600 N9 GUA F 4 3.113 15.662 13.184 1.00 32.40 F N ATOM 1601 C8 GUA F 4 3.178 14.408 13.743 1.00 30.83 F C ATOM 1602 N7 GUA F 4 4.226 13.724 13.367 1.00 30.41 F N ATOM 1603 C5 GUA F 4 4.907 14.581 12.507 1.00 30.17 F C ATOM 1604 C6 GUA F 4 6.116 14.396 11.787 1.00 27.54 F C ATOM 1605 O6 GUA F 4 6.864 13.403 11.757 1.00 25.09 F O ATOM 1606 N1 GUA F 4 6.442 15.526 11.041 1.00 28.44 F N ATOM 1607 C2 GUA F 4 5.697 16.679 10.991 1.00 31.59 F C ATOM 1608 N2 GUA F 4 6.170 17.660 10.212 1.00 36.28 F N ATOM 1609 N3 GUA F 4 4.567 16.866 11.657 1.00 30.17 F N ATOM 1610 C4 GUA F 4 4.234 15.778 12.391 1.00 31.30 F C ATOM 1611 P CYT F 5 −1.174 18.766 11.913 1.00 55.22 F P ATOM 1612 OP1 CYT F 5 −1.967 20.000 12.116 1.00 35.41 F O ATOM 1613 OP2 CYT F 5 −1.818 17.463 11.625 1.00 41.84 F O ATOM 1614 O5′ CYT F 5 −0.117 19.042 10.750 1.00 45.09 F O ATOM 1615 C5′ CYT F 5 0.805 20.099 10.935 1.00 36.95 F C ATOM 1616 C4′ CYT F 5 1.679 20.233 9.710 1.00 34.80 F C ATOM 1617 O4′ CYT F 5 2.599 19.115 9.620 1.00 30.71 F O ATOM 1618 C3′ CYT F 5 0.917 20.269 8.395 1.00 32.81 F C ATOM 1619 O3′ CYT F 5 1.552 21.256 7.611 1.00 38.98 F O ATOM 1620 C2′ CYT F 5 1.090 18.847 7.850 1.00 30.04 F C ATOM 1621 C1′ CYT F 5 2.483 18.494 8.360 1.00 30.96 F C ATOM 1622 N1 CYT F 5 2.763 17.057 8.621 1.00 32.68 F N ATOM 1623 C2 CYT F 5 3.866 16.455 8.007 1.00 28.42 F C ATOM 1624 O2 CYT F 5 4.574 17.122 7.239 1.00 30.64 F O ATOM 1625 N3 CYT F 5 4.129 15.152 8.271 1.00 29.28 F N ATOM 1626 C4 CYT F 5 3.344 14.461 9.101 1.00 28.82 F C ATOM 1627 N4 CYT F 5 3.652 13.176 9.319 1.00 26.68 F N ATOM 1628 C5 CYT F 5 2.218 15.058 9.741 1.00 26.50 F C ATOM 1629 C6 CYT F 5 1.973 16.347 9.477 1.00 34.18 F C ATOM 1630 P THY F 6 0.911 21.797 6.257 1.00 45.82 F P ATOM 1631 OP1 THY F 6 1.340 23.204 6.087 1.00 50.17 F O ATOM 1632 OP2 THY F 6 −0.527 21.445 6.242 1.00 48.70 F O ATOM 1633 O5′ THY F 6 1.645 20.899 5.156 1.00 45.06 F O ATOM 1634 C5′ THY F 6 2.993 21.162 4.785 1.00 41.65 F C ATOM 1635 C4′ THY F 6 3.362 20.354 3.556 1.00 37.82 F C ATOM 1636 O4′ THY F 6 3.682 18.997 3.962 1.00 40.57 F O ATOM 1637 C3′ THY F 6 2.234 20.213 2.540 1.00 38.89 F C ATOM 1638 O3′ THY F 6 2.758 19.997 1.240 1.00 45.07 F O ATOM 1639 C2′ THY F 6 1.555 18.940 3.018 1.00 39.65 F C ATOM 1640 C1′ THY F 6 2.810 18.118 3.277 1.00 40.46 F C ATOM 1641 N1 THY F 6 2.575 16.902 4.089 1.00 33.12 F N ATOM 1642 C2 THY F 6 3.531 15.917 4.063 1.00 33.34 F C ATOM 1643 O2 THY F 6 4.553 16.018 3.409 1.00 36.26 F O ATOM 1644 N3 THY F 6 3.244 14.819 4.836 1.00 29.65 F N ATOM 1645 C4 THY F 6 2.113 14.623 5.607 1.00 30.16 F C ATOM 1646 O4 THY F 6 1.944 13.601 6.265 1.00 28.94 F O ATOM 1647 C5 THY F 6 1.146 15.697 5.580 1.00 31.04 F C ATOM 1648 C7 THY F 6 −0.125 15.596 6.376 1.00 27.30 F C ATOM 1649 C6 THY F 6 1.420 16.773 4.831 1.00 29.41 F C ATOM 1650 P ADE F 7 3.087 21.237 0.286 1.00 43.24 F P ATOM 1651 OP1 ADE F 7 3.511 22.361 1.152 1.00 39.52 F O ATOM 1652 OP2 ADE F 7 1.946 21.410 −0.641 1.00 43.23 F O ATOM 1653 O5′ ADE F 7 4.337 20.696 −0.558 1.00 31.77 F O ATOM 1654 C5′ ADE F 7 5.573 20.439 0.091 1.00 31.76 F C ATOM 1655 C4′ ADE F 7 6.250 19.186 −0.442 1.00 34.10 F C ATOM 1656 O4′ ADE F 7 5.668 17.997 0.158 1.00 36.40 F O ATOM 1657 C3′ ADE F 7 6.159 18.965 −1.945 1.00 37.37 F C ATOM 1658 O3′ ADE F 7 7.365 18.325 −2.375 1.00 37.11 F O ATOM 1659 C2′ ADE F 7 4.922 18.068 −2.076 1.00 34.22 F C ATOM 1660 C1′ ADE F 7 5.045 17.190 −0.831 1.00 36.46 F C ATOM 1661 N9 ADE F 7 3.796 16.716 −0.234 1.00 29.12 F N ATOM 1662 C8 ADE F 7 2.603 17.380 −0.136 1.00 31.32 F C ATOM 1663 N7 ADE F 7 1.664 16.695 0.484 1.00 32.25 F N ATOM 1664 C5 ADE F 7 2.284 15.502 0.826 1.00 26.57 F C ATOM 1665 C6 ADE F 7 1.838 14.346 1.503 1.00 22.11 F C ATOM 1666 N6 ADE F 7 0.599 14.190 1.983 1.00 20.31 F N ATOM 1667 N1 ADE F 7 2.723 13.340 1.670 1.00 22.14 F N ATOM 1668 C2 ADE F 7 3.964 13.483 1.198 1.00 23.50 F C ATOM 1669 N3 ADE F 7 4.500 14.518 0.551 1.00 28.66 F N ATOM 1670 C4 ADE F 7 3.601 15.505 0.395 1.00 30.88 F C ATOM 1671 P ADE F 8 7.584 17.995 −3.924 1.00 57.47 F P ATOM 1672 OP1 ADE F 8 9.025 18.154 −4.225 1.00 44.64 F O ATOM 1673 OP2 ADE F 8 6.546 18.735 −4.687 1.00 39.39 F O ATOM 1674 O5′ ADE F 8 7.234 16.441 −4.011 1.00 40.95 F O ATOM 1675 C5′ ADE F 8 7.986 15.526 −3.241 1.00 40.65 F C ATOM 1676 C4′ ADE F 8 7.318 14.166 −3.261 1.00 42.55 F C ATOM 1677 O4′ ADE F 8 6.068 14.237 −2.542 1.00 43.82 F O ATOM 1678 C3′ ADE F 8 6.962 13.635 −4.648 1.00 37.24 F C ATOM 1679 O3′ ADE F 8 7.876 12.598 −4.962 1.00 36.02 F O ATOM 1680 C2′ ADE F 8 5.523 13.126 −4.513 1.00 34.48 F C ATOM 1681 C1′ ADE F 8 5.279 13.168 −3.007 1.00 36.61 F C ATOM 1682 N9 ADE F 8 3.897 13.418 −2.605 1.00 35.16 F N ATOM 1683 C8 ADE F 8 3.136 14.523 −2.874 1.00 34.63 F C ATOM 1684 N7 ADE F 8 1.924 14.470 −2.372 1.00 33.52 F N ATOM 1685 C5 ADE F 8 1.890 13.243 −1.730 1.00 30.78 F C ATOM 1686 C6 ADE F 8 0.881 12.586 −1.000 1.00 36.08 F C ATOM 1687 N6 ADE F 8 −0.330 13.117 −0.802 1.00 31.29 F N ATOM 1688 N1 ADE F 8 1.168 11.366 −0.482 1.00 34.00 F N ATOM 1689 C2 ADE F 8 2.390 10.849 −0.691 1.00 37.64 F C ATOM 1690 N3 ADE F 8 3.421 11.372 −1.364 1.00 31.88 F N ATOM 1691 C4 ADE F 8 3.099 12.581 −1.860 1.00 32.34 F C ATOM 1692 P THY F 9 7.678 11.637 −6.223 1.00 38.24 F P ATOM 1693 OP1 THY F 9 9.021 11.281 −6.729 1.00 31.02 F O ATOM 1694 OP2 THY F 9 6.669 12.226 −7.135 1.00 36.79 F O ATOM 1695 O5′ THY F 9 7.060 10.340 −5.528 1.00 35.06 F O ATOM 1696 C5′ THY F 9 7.848 9.687 −4.551 1.00 35.57 F C ATOM 1697 C4′ THY F 9 7.066 8.560 −3.913 1.00 34.01 F C ATOM 1698 O4′ THY F 9 5.808 9.079 −3.419 1.00 27.93 F O ATOM 1699 C3′ THY F 9 6.722 7.390 −4.832 1.00 28.47 F C ATOM 1700 O3′ THY F 9 6.955 6.202 −4.082 1.00 28.04 F O ATOM 1701 C2′ THY F 9 5.248 7.620 −5.164 1.00 26.35 F C ATOM 1702 C1′ THY F 9 4.753 8.259 −3.869 1.00 27.34 F C ATOM 1703 N1 THY F 9 3.561 9.140 −3.995 1.00 25.52 F N ATOM 1704 C2 THY F 9 2.512 8.921 −3.143 1.00 27.45 F C ATOM 1705 O2 THY F 9 2.528 8.038 −2.306 1.00 29.33 F O ATOM 1706 N3 THY F 9 1.451 9.776 −3.308 1.00 28.84 F N ATOM 1707 C4 THY F 9 1.345 10.805 −4.226 1.00 26.17 F C ATOM 1708 O4 THY F 9 0.357 11.526 −4.310 1.00 27.50 F O ATOM 1709 C5 THY F 9 2.477 10.978 −5.088 1.00 27.41 F C ATOM 1710 C7 THY F 9 2.450 12.071 −6.119 1.00 26.72 F C ATOM 1711 C6 THY F 9 3.522 10.151 −4.933 1.00 27.85 F C ATOM 1712 P ADE F 10 6.614 4.738 −4.629 1.00 23.93 F P ATOM 1713 OP1 ADE F 10 7.397 3.770 −3.830 1.00 23.75 F O ATOM 1714 OP2 ADE F 10 6.742 4.742 −6.104 1.00 31.81 F O ATOM 1715 O5′ ADE F 10 5.071 4.571 −4.220 1.00 35.82 F O ATOM 1716 C5′ ADE F 10 4.732 4.500 −2.835 1.00 25.94 F C ATOM 1717 C4′ ADE F 10 3.369 3.873 −2.576 1.00 20.59 F C ATOM 1718 O4′ ADE F 10 2.313 4.838 −2.795 1.00 22.02 F O ATOM 1719 C3′ ADE F 10 2.998 2.665 −3.428 1.00 25.03 F C ATOM 1720 O3′ ADE F 10 2.352 1.741 −2.564 1.00 21.68 F O ATOM 1721 C2′ ADE F 10 2.059 3.247 −4.486 1.00 20.64 F C ATOM 1722 C1′ ADE F 10 1.340 4.328 −3.686 1.00 21.60 F C ATOM 1723 N9 ADE F 10 0.878 5.487 −4.447 1.00 24.05 F N ATOM 1724 C8 ADE F 10 1.593 6.194 −5.377 1.00 20.24 F C ATOM 1725 N7 ADE F 10 0.930 7.207 −5.882 1.00 22.47 F N ATOM 1726 C5 ADE F 10 −0.296 7.166 −5.240 1.00 19.26 F C ATOM 1727 C6 ADE F 10 −1.445 7.976 −5.337 1.00 21.91 F C ATOM 1728 N6 ADE F 10 −1.537 9.028 −6.159 1.00 22.42 F N ATOM 1729 N1 ADE F 10 −2.502 7.663 −4.556 1.00 20.46 F N ATOM 1730 C2 ADE F 10 −2.404 6.608 −3.738 1.00 21.25 F C ATOM 1731 N3 ADE F 10 −1.373 5.777 −3.557 1.00 21.22 F N ATOM 1732 C4 ADE F 10 −0.343 6.115 −4.348 1.00 18.15 F C ATOM 1733 P ADE F 11 1.831 0.323 −3.073 1.00 26.26 F P ATOM 1734 OP1 ADE F 11 2.148 −0.677 −2.034 1.00 33.89 F O ATOM 1735 OP2 ADE F 11 2.267 0.111 −4.472 1.00 23.71 F O ATOM 1736 O5′ ADE F 11 0.251 0.571 −3.069 1.00 30.04 F O ATOM 1737 C5′ ADE F 11 −0.359 1.033 −1.884 1.00 23.86 F C ATOM 1738 C4′ ADE F 11 −1.850 1.245 −2.067 1.00 25.98 F C ATOM 1739 O4′ ADE F 11 −2.088 2.375 −2.942 1.00 21.87 F O ATOM 1740 C3′ ADE F 11 −2.629 0.077 −2.661 1.00 27.40 F C ATOM 1741 O3′ ADE F 11 −3.869 0.048 −1.963 1.00 27.22 F O ATOM 1742 C2′ ADE F 11 −2.785 0.484 −4.126 1.00 22.69 F C ATOM 1743 C1′ ADE F 11 −2.949 1.997 −3.991 1.00 25.23 F C ATOM 1744 N9 ADE F 11 −2.484 2.813 −5.103 1.00 25.79 F N ATOM 1745 C8 ADE F 11 −1.310 2.670 −5.794 1.00 25.41 F C ATOM 1746 N7 ADE F 11 −1.138 3.568 −6.736 1.00 26.27 F N ATOM 1747 C5 ADE F 11 −2.274 4.357 −6.639 1.00 24.40 F C ATOM 1748 C6 ADE F 11 −2.693 5.484 −7.361 1.00 26.97 F C ATOM 1749 N6 ADE F 11 −1.962 6.001 −8.355 1.00 30.79 F N ATOM 1750 N1 ADE F 11 −3.880 6.043 −7.028 1.00 26.76 F N ATOM 1751 C2 ADE F 11 −4.594 5.498 −6.030 1.00 27.39 F C ATOM 1752 N3 ADE F 11 −4.296 4.433 −5.279 1.00 24.26 F N ATOM 1753 C4 ADE F 11 −3.113 3.912 −5.638 1.00 22.08 F C ATOM 1754 P THY F 12 −4.857 −1.211 −1.981 1.00 26.75 F P ATOM 1755 OP1 THY F 12 −5.433 −1.311 −0.619 1.00 27.03 F O ATOM 1756 OP2 THY F 12 −4.163 −2.383 −2.556 1.00 22.77 F O ATOM 1757 O5′ THY F 12 −5.993 −0.716 −2.998 1.00 26.06 F O ATOM 1758 C5′ THY F 12 −6.803 0.411 −2.603 1.00 24.65 F C ATOM 1759 C4′ THY F 12 −7.609 0.986 −3.754 1.00 27.12 F C ATOM 1760 O4′ THY F 12 −6.751 1.762 −4.633 1.00 24.99 F O ATOM 1761 C3′ THY F 12 −8.307 −0.047 −4.646 1.00 27.27 F C ATOM 1762 O3′ THY F 12 −9.654 0.322 −4.869 1.00 26.89 F O ATOM 1763 C2′ THY F 12 −7.524 0.037 −5.955 1.00 22.09 F C ATOM 1764 C1′ THY F 12 −7.222 1.528 −5.945 1.00 23.77 F C ATOM 1765 N1 THY F 12 −6.198 1.950 −6.926 1.00 23.74 F N ATOM 1766 C2 THY F 12 −6.346 3.165 −7.564 1.00 24.23 F C ATOM 1767 O2 THY F 12 −7.277 3.925 −7.363 1.00 22.95 F O ATOM 1768 N3 THY F 12 −5.346 3.463 −8.452 1.00 21.71 F N ATOM 1769 C4 THY F 12 −4.250 2.684 −8.753 1.00 21.38 F C ATOM 1770 O4 THY F 12 −3.416 3.055 −9.568 1.00 26.86 F O ATOM 1771 C5 THY F 12 −4.161 1.425 −8.051 1.00 19.72 F C ATOM 1772 C7 THY F 12 −3.013 0.485 −8.294 1.00 20.68 F C ATOM 1773 C6 THY F 12 −5.128 1.120 −7.183 1.00 19.97 F C ATOM 1774 P ADE F 13 −10.808 0.035 −3.799 1.00 37.17 F P ATOM 1775 OP1 ADE F 13 −10.428 0.709 −2.533 1.00 31.49 F O ATOM 1776 OP2 ADE F 13 −11.117 −1.414 −3.821 1.00 25.92 F O ATOM 1777 O5′ ADE F 13 −12.042 0.827 −4.445 1.00 33.97 F O ATOM 1778 C5′ ADE F 13 −12.010 2.251 −4.451 1.00 31.66 F C ATOM 1779 C4′ ADE F 13 −12.914 2.837 −5.523 1.00 36.86 F C ATOM 1780 O4′ ADE F 13 −12.183 3.096 −6.750 1.00 31.85 F O ATOM 1781 C3′ ADE F 13 −14.115 1.994 −5.925 1.00 27.27 F C ATOM 1782 O3′ ADE F 13 −15.155 2.910 −6.228 1.00 29.73 F O ATOM 1783 C2′ ADE F 13 −13.604 1.237 −7.148 1.00 26.25 F C ATOM 1784 C1′ ADE F 13 −12.558 2.173 −7.754 1.00 29.08 F C ATOM 1785 N9 ADE F 13 −11.324 1.523 −8.187 1.00 25.69 F N ATOM 1786 C8 ADE F 13 −10.877 0.272 −7.861 1.00 22.17 F C ATOM 1787 N7 ADE F 13 −9.718 −0.031 −8.405 1.00 23.97 F N ATOM 1788 C5 ADE F 13 −9.372 1.106 −9.123 1.00 22.53 F C ATOM 1789 C6 ADE F 13 −8.249 1.433 −9.914 1.00 23.42 F C ATOM 1790 N6 ADE F 13 −7.222 0.600 −10.129 1.00 20.47 F N ATOM 1791 N1 ADE F 13 −8.224 2.655 −10.485 1.00 23.63 F N ATOM 1792 C2 ADE F 13 −9.251 3.487 −10.274 1.00 24.20 F C ATOM 1793 N3 ADE F 13 −10.355 3.295 −9.551 1.00 24.43 F N ATOM 1794 C4 ADE F 13 −10.352 2.074 −8.994 1.00 23.99 F C ATOM 1795 P GUA F 14 −16.572 2.450 −6.800 1.00 30.58 F P ATOM 1796 OP1 GUA F 14 −17.581 3.404 −6.283 1.00 29.22 F O ATOM 1797 OP2 GUA F 14 −16.732 0.996 −6.558 1.00 28.14 F O ATOM 1798 O5′ GUA F 14 −16.417 2.710 −8.369 1.00 21.73 F O ATOM 1799 C5′ GUA F 14 −16.239 4.053 −8.799 1.00 28.86 F C ATOM 1800 C4′ GUA F 14 −15.866 4.106 −10.267 1.00 35.27 F C ATOM 1801 O4′ GUA F 14 −14.568 3.491 −10.468 1.00 32.56 F O ATOM 1802 C3′ GUA F 14 −16.849 3.401 −11.197 1.00 41.42 F C ATOM 1803 O3′ GUA F 14 −17.292 4.357 −12.165 1.00 50.72 F O ATOM 1804 C2′ GUA F 14 −16.046 2.239 −11.786 1.00 35.19 F C ATOM 1805 C1′ GUA F 14 −14.601 2.711 −11.636 1.00 28.95 F C ATOM 1806 N9 GUA F 14 −13.629 1.628 −11.502 1.00 28.65 F N ATOM 1807 C8 GUA F 14 −13.734 0.478 −10.751 1.00 27.50 F C ATOM 1808 N7 GUA F 14 −12.690 −0.305 −10.845 1.00 25.21 F N ATOM 1809 C5 GUA F 14 −11.835 0.372 −11.706 1.00 22.23 F C ATOM 1810 C6 GUA F 14 −10.554 0.025 −12.185 1.00 23.99 F C ATOM 1811 O6 GUA F 14 −9.894 −0.990 −11.930 1.00 26.66 F O ATOM 1812 N1 GUA F 14 −10.039 0.991 −13.050 1.00 23.15 F N ATOM 1813 C2 GUA F 14 −10.683 2.153 −13.402 1.00 27.10 F C ATOM 1814 N2 GUA F 14 −10.040 2.977 −14.244 1.00 27.62 F N ATOM 1815 N3 GUA F 14 −11.882 2.492 −12.955 1.00 29.89 F N ATOM 1816 C4 GUA F 14 −12.397 1.559 −12.118 1.00 28.73 F C ATOM 1817 P CYT F 15 −17.994 3.944 −13.540 1.00 57.53 F P ATOM 1818 OP1 CYT F 15 −18.880 5.065 −13.912 1.00 66.77 F O ATOM 1819 OP2 CYT F 15 −18.533 2.569 −13.429 1.00 45.10 F O ATOM 1820 O5′ CYT F 15 −16.765 3.919 −14.561 1.00 61.13 F O ATOM 1821 C5′ CYT F 15 −16.011 5.107 −14.774 1.00 60.71 F C ATOM 1822 C4′ CYT F 15 −14.957 4.886 −15.844 1.00 63.70 F C ATOM 1823 O4′ CYT F 15 −14.016 3.870 −15.408 1.00 56.35 F O ATOM 1824 C3′ CYT F 15 −15.507 4.415 −17.186 1.00 63.78 F C ATOM 1825 O3′ CYT F 15 −14.833 5.094 −18.244 1.00 69.14 F O ATOM 1826 C2′ CYT F 15 −15.220 2.915 −17.180 1.00 54.75 F C ATOM 1827 C1′ CYT F 15 −13.925 2.848 −16.379 1.00 50.07 F C ATOM 1828 N1 CYT F 15 −13.730 1.550 −15.671 1.00 42.12 F N ATOM 1829 C2 CYT F 15 −12.553 0.820 −15.884 1.00 38.81 F C ATOM 1830 O2 CYT F 15 −11.691 1.262 −16.660 1.00 38.49 F O ATOM 1831 N3 CYT F 15 −12.390 −0.357 −15.231 1.00 32.50 F N ATOM 1832 C4 CYT F 15 −13.338 −0.803 −14.404 1.00 36.68 F C ATOM 1833 N4 CYT F 15 −13.119 −1.972 −13.789 1.00 32.28 F N ATOM 1834 C5 CYT F 15 −14.546 −0.071 −14.174 1.00 36.00 F C ATOM 1835 C6 CYT F 15 −14.696 1.089 −14.822 1.00 37.43 F C ATOM 1836 P THY F 16 −15.377 5.023 −19.751 1.00 80.16 F P ATOM 1837 OP1 THY F 16 −15.380 6.409 −20.269 1.00 68.74 F O ATOM 1838 OP2 THY F 16 −16.614 4.202 −19.786 1.00 59.17 F O ATOM 1839 O5′ THY F 16 −14.242 4.186 −20.504 1.00 74.20 F O ATOM 1840 C5′ THY F 16 −12.868 4.527 −20.356 1.00 64.50 F C ATOM 1841 C4′ THY F 16 −12.005 3.433 −20.959 1.00 61.48 F C ATOM 1842 O4′ THY F 16 −11.933 2.288 −20.071 1.00 56.08 F O ATOM 1843 C3′ THY F 16 −12.522 2.903 −22.292 1.00 64.84 F C ATOM 1844 O3′ THY F 16 −11.448 2.856 −23.218 1.00 65.11 F O ATOM 1845 C2′ THY F 16 −13.065 1.514 −21.959 1.00 58.52 F C ATOM 1846 C1′ THY F 16 −12.146 1.106 −20.816 1.00 48.55 F C ATOM 1847 N1 THY F 16 −12.712 0.088 −19.887 1.00 44.56 F N ATOM 1848 C2 THY F 16 −11.930 −0.987 −19.523 1.00 41.93 F C ATOM 1849 O2 THY F 16 −10.789 −1.154 −19.928 1.00 36.72 F O ATOM 1850 N3 THY F 16 −12.540 −1.862 −18.658 1.00 37.33 F N ATOM 1851 C4 THY F 16 −13.817 −1.771 −18.138 1.00 38.23 F C ATOM 1852 O4 THY F 16 −14.279 −2.606 −17.367 1.00 38.67 F O ATOM 1853 C5 THY F 16 −14.576 −0.625 −18.564 1.00 39.50 F C ATOM 1854 C7 THY F 16 −15.975 −0.438 −18.059 1.00 37.21 F C ATOM 1855 C6 THY F 16 −13.998 0.241 −19.406 1.00 43.36 F C ATOM 1856 P THY F 17 −11.767 2.951 −24.778 1.00 81.71 F P ATOM 1857 OP1 THY F 17 −10.777 3.861 −25.394 1.00 56.22 F O ATOM 1858 OP2 THY F 17 −13.218 3.216 −24.919 1.00 75.03 F O ATOM 1859 O5′ THY F 17 −11.493 1.459 −25.283 1.00 76.85 F O ATOM 1860 C5′ THY F 17 −10.171 0.932 −25.289 1.00 71.22 F C ATOM 1861 C4′ THY F 17 −10.213 −0.575 −25.471 1.00 71.63 F C ATOM 1862 O4′ THY F 17 −10.789 −1.183 −24.287 1.00 63.05 F O ATOM 1863 C3′ THY F 17 −11.042 −1.060 −26.661 1.00 64.78 F C ATOM 1864 O3′ THY F 17 −10.284 −1.985 −27.435 1.00 63.87 F O ATOM 1865 C2′ THY F 17 −12.265 −1.721 −26.025 1.00 64.01 F C ATOM 1866 C1′ THY F 17 −11.714 −2.172 −24.678 1.00 67.24 F C ATOM 1867 N1 THY F 17 −12.743 −2.246 −23.624 1.00 64.24 F N ATOM 1868 C2 THY F 17 −12.611 −3.176 −22.614 1.00 58.85 F C ATOM 1869 O2 THY F 17 −11.674 −3.955 −22.540 1.00 48.20 F O ATOM 1870 N3 THY F 17 −13.627 −3.153 −21.689 1.00 46.71 F N ATOM 1871 C4 THY F 17 −14.726 −2.314 −21.681 1.00 48.10 F C ATOM 1872 O4 THY F 17 −15.585 −2.370 −20.808 1.00 54.41 F O ATOM 1873 C5 THY F 17 −14.795 −1.367 −22.768 1.00 57.18 F C ATOM 1874 C7 THY F 17 −15.944 −0.406 −22.864 1.00 61.07 F C ATOM 1875 C6 THY F 17 −13.813 −1.379 −23.678 1.00 62.83 F C TER ATOM 1876 N GLY C 2 26.102 −30.410 −22.106 1.00 37.16 C N ATOM 1877 CA GLY C 2 27.225 −30.891 −22.889 1.00 37.40 C C ATOM 1878 C GLY C 2 27.997 −31.989 −22.183 1.00 41.01 C C ATOM 1879 O GLY C 2 27.938 −32.110 −20.958 1.00 42.86 C O ATOM 1880 N ARG C 3 28.721 −32.793 −22.956 1.00 39.84 C N ATOM 1881 CA ARG C 3 29.520 −33.876 −22.393 1.00 40.18 C C ATOM 1882 C ARG C 3 30.538 −33.327 −21.398 1.00 43.21 C C ATOM 1883 O ARG C 3 30.820 −33.945 −20.369 1.00 45.60 C O ATOM 1884 CB ARG C 3 30.219 −34.661 −23.504 1.00 39.06 C C ATOM 1885 CG ARG C 3 29.272 −35.479 −24.372 1.00 38.76 C C ATOM 1886 CD ARG C 3 28.414 −36.403 −23.522 1.00 43.44 C C ATOM 1887 NE ARG C 3 27.577 −37.286 −24.330 1.00 39.28 C N ATOM 1888 CZ ARG C 3 27.994 −38.428 −24.868 1.00 44.32 C C ATOM 1889 NH1 ARG C 3 29.247 −38.828 −24.698 1.00 35.70 C N ATOM 1890 NH2 ARG C 3 27.159 −39.167 −25.583 1.00 41.27 C N ATOM 1891 N LYS C 4 31.082 −32.159 −21.716 1.00 38.21 C N ATOM 1892 CA LYS C 4 31.986 −31.455 −20.817 1.00 40.07 C C ATOM 1893 C LYS C 4 31.589 −29.985 −20.733 1.00 44.07 C C ATOM 1894 O LYS C 4 31.123 −29.404 −21.713 1.00 36.32 C O ATOM 1895 CB LYS C 4 33.437 −31.575 −21.299 1.00 41.27 C C ATOM 1896 CG LYS C 4 34.023 −32.977 −21.180 1.00 43.87 C C ATOM 1897 CD LYS C 4 33.886 −33.497 −19.754 1.00 44.62 C C ATOM 1898 CE LYS C 4 33.899 −35.016 −19.705 1.00 58.07 C C ATOM 1899 NZ LYS C 4 33.253 −35.524 −18.459 1.00 51.82 C N ATOM 1900 N LYS C 5 31.768 −29.387 −19.561 1.00 44.47 C N ATOM 1901 CA LYS C 5 31.606 −27.947 −19.433 1.00 41.82 C C ATOM 1902 C LYS C 5 32.702 −27.261 −20.233 1.00 44.25 C C ATOM 1903 O LYS C 5 33.806 −27.791 −20.359 1.00 49.21 C O ATOM 1904 CB LYS C 5 31.682 −27.513 −17.971 1.00 39.15 C C ATOM 1905 CG LYS C 5 31.691 −26.002 −17.792 1.00 46.63 C C ATOM 1906 CD LYS C 5 31.374 −25.594 −16.363 1.00 42.50 C C ATOM 1907 CE LYS C 5 31.225 −24.090 −16.258 1.00 46.51 C C ATOM 1908 NZ LYS C 5 30.818 −23.663 −14.892 1.00 51.90 C N ATOM 1909 N ILE C 6 32.398 −26.089 −20.782 1.00 37.05 C N ATOM 1910 CA ILE C 6 33.394 −25.321 −21.521 1.00 35.04 C C ATOM 1911 C ILE C 6 33.581 −23.914 −20.958 1.00 40.67 C C ATOM 1912 O ILE C 6 32.791 −23.446 −20.136 1.00 41.66 C O ATOM 1913 CB ILE C 6 33.041 −25.223 −23.013 1.00 38.26 C C ATOM 1914 CG1 ILE C 6 31.877 −24.255 −23.235 1.00 33.65 C C ATOM 1915 CG2 ILE C 6 32.721 −26.603 −23.569 1.00 41.12 C C ATOM 1916 CD1 ILE C 6 31.712 −23.841 −24.682 1.00 34.76 C C ATOM 1917 N GLN C 7 34.644 −23.249 −21.396 1.00 46.96 C N ATOM 1918 CA GLN C 7 34.892 −21.873 −20.999 1.00 46.22 C C ATOM 1919 C GLN C 7 34.452 −20.956 −22.120 1.00 44.41 C C ATOM 1920 O GLN C 7 34.662 −21.257 −23.296 1.00 43.97 C O ATOM 1921 CB GLN C 7 36.374 −21.649 −20.687 1.00 54.97 C C ATOM 1922 CG GLN C 7 36.843 −22.323 −19.409 1.00 57.18 C C ATOM 1923 CD GLN C 7 35.980 −21.963 −18.213 1.00 73.60 C C ATOM 1924 OE1 GLN C 7 35.636 −20.797 −18.008 1.00 77.65 C O ATOM 1925 NE2 GLN C 7 35.629 −22.966 −17.413 1.00 72.99 C N ATOM 1926 N ILE C 8 33.830 −19.839 −21.761 1.00 28.39 C N ATOM 1927 CA ILE C 8 33.363 −18.899 −22.767 1.00 21.10 C C ATOM 1928 C ILE C 8 34.548 −18.138 −23.353 1.00 24.35 C C ATOM 1929 O ILE C 8 34.920 −17.062 −22.879 1.00 25.10 C O ATOM 1930 CB ILE C 8 32.292 −17.944 −22.211 1.00 20.86 C C ATOM 1931 CG1 ILE C 8 31.062 −18.743 −21.773 1.00 27.03 C C ATOM 1932 CG2 ILE C 8 31.895 −16.916 −23.249 1.00 18.08 C C ATOM 1933 CD1 ILE C 8 30.547 −19.712 −22.835 1.00 21.56 C C ATOM 1934 N THR C 9 35.149 −18.718 −24.386 1.00 18.31 C N ATOM 1935 CA THR C 9 36.265 −18.074 −25.064 1.00 18.73 C C ATOM 1936 C THR C 9 36.330 −18.510 −26.528 1.00 16.20 C C ATOM 1937 O THR C 9 35.998 −19.652 −26.865 1.00 19.80 C O ATOM 1938 CB THR C 9 37.604 −18.337 −24.335 1.00 22.75 C C ATOM 1939 OG1 THR C 9 38.643 −17.538 −24.920 1.00 29.46 C O ATOM 1940 CG2 THR C 9 37.976 −19.817 −24.395 1.00 15.15 C C ATOM 1941 N ARG C 10 36.736 −17.577 −27.385 1.00 22.69 C N ATOM 1942 CA ARG C 10 36.805 −17.797 −28.828 1.00 28.13 C C ATOM 1943 C ARG C 10 37.364 −19.165 −29.205 1.00 26.44 C C ATOM 1944 O ARG C 10 38.497 −19.501 −28.866 1.00 27.25 C O ATOM 1945 CB ARG C 10 37.635 −16.698 −29.496 1.00 25.83 C C ATOM 1946 CG ARG C 10 37.636 −16.769 −31.009 1.00 25.49 C C ATOM 1947 CD ARG C 10 38.512 −15.688 −31.619 1.00 26.19 C C ATOM 1948 NE ARG C 10 38.533 −15.776 −33.077 1.00 42.34 C N ATOM 1949 CZ ARG C 10 39.313 −16.606 −33.764 1.00 35.92 C C ATOM 1950 NH1 ARG C 10 40.138 −17.421 −33.123 1.00 40.43 C N ATOM 1951 NH2 ARG C 10 39.269 −16.620 −35.089 1.00 33.33 C N ATOM 1952 N ILE C 11 36.546 −19.948 −29.898 1.00 13.48 C N ATOM 1953 CA ILE C 11 36.954 −21.246 −30.411 1.00 16.65 C C ATOM 1954 C ILE C 11 37.985 −21.029 −31.516 1.00 20.36 C C ATOM 1955 O ILE C 11 37.745 −20.268 −32.458 1.00 21.24 C O ATOM 1956 CB ILE C 11 35.741 −22.022 −30.952 1.00 21.38 C C ATOM 1957 CG1 ILE C 11 34.750 −22.296 −29.816 1.00 14.80 C C ATOM 1958 CG2 ILE C 11 36.177 −23.320 −31.635 1.00 14.57 C C ATOM 1959 CD1 ILE C 11 33.463 −22.954 −30.264 1.00 16.69 C C ATOM 1960 N MET C 12 39.138 −21.678 −31.382 1.00 22.82 C N ATOM 1961 CA MET C 12 40.267 −21.407 −32.262 1.00 29.62 C C ATOM 1962 C MET C 12 40.202 −22.231 −33.544 1.00 29.22 C C ATOM 1963 O MET C 12 40.707 −21.810 −34.581 1.00 28.51 C O ATOM 1964 CB MET C 12 41.594 −21.653 −31.533 1.00 24.77 C C ATOM 1965 CG MET C 12 41.796 −20.801 −30.272 1.00 29.84 C C ATOM 1966 SD MET C 12 41.935 −19.026 −30.587 1.00 31.80 C S ATOM 1967 CE MET C 12 43.472 −18.972 −31.519 1.00 25.97 C C ATOM 1968 N ASP C 13 39.577 −23.401 −33.461 1.00 47.38 C N ATOM 1969 CA ASP C 13 39.448 −24.301 −34.604 1.00 49.89 C C ATOM 1970 C ASP C 13 38.251 −23.913 −35.472 1.00 45.31 C C ATOM 1971 O ASP C 13 37.102 −24.017 −35.041 1.00 43.32 C O ATOM 1972 CB ASP C 13 39.301 −25.745 −34.114 1.00 49.98 C C ATOM 1973 CG ASP C 13 38.903 −26.707 −35.223 1.00 66.17 C C ATOM 1974 OD1 ASP C 13 39.467 −26.610 −36.335 1.00 72.90 C O ATOM 1975 OD2 ASP C 13 38.030 −27.571 −34.979 1.00 61.32 C O ATOM 1976 N GLU C 14 38.530 −23.461 −36.690 1.00 27.77 C N ATOM 1977 CA GLU C 14 37.488 −23.055 −37.629 1.00 33.41 C C ATOM 1978 C GLU C 14 36.413 −24.122 −37.807 1.00 38.75 C C ATOM 1979 O GLU C 14 35.233 −23.808 −37.960 1.00 31.01 C O ATOM 1980 CB GLU C 14 38.096 −22.710 −38.991 1.00 30.94 C C ATOM 1981 CG GLU C 14 37.079 −22.438 −40.088 1.00 33.31 C C ATOM 1982 CD GLU C 14 37.732 −22.114 −41.426 1.00 61.19 C C ATOM 1983 OE1 GLU C 14 38.831 −22.642 −41.705 1.00 66.85 C O ATOM 1984 OE2 GLU C 14 37.144 −21.333 −42.204 1.00 51.72 C O ATOM 1985 N ARG C 15 36.816 −25.386 −37.785 1.00 49.66 C N ATOM 1986 CA ARG C 15 35.856 −26.464 −37.972 1.00 42.37 C C ATOM 1987 C ARG C 15 34.830 −26.496 −36.843 1.00 37.98 C C ATOM 1988 O ARG C 15 33.637 −26.352 −37.088 1.00 34.22 C O ATOM 1989 CB ARG C 15 36.562 −27.814 −38.111 1.00 51.26 C C ATOM 1990 CG ARG C 15 35.704 −28.875 −38.771 1.00 56.80 C C ATOM 1991 CD ARG C 15 36.503 −29.690 −39.775 1.00 67.79 C C ATOM 1992 NE ARG C 15 35.708 −29.979 −40.966 1.00 74.25 C N ATOM 1993 CZ ARG C 15 35.568 −29.141 −41.990 1.00 70.71 C C ATOM 1994 NH1 ARG C 15 36.173 −27.959 −41.971 1.00 78.90 C N ATOM 1995 NH2 ARG C 15 34.822 −29.481 −43.035 1.00 52.78 C N ATOM 1996 N ASN C 16 35.292 −26.677 −35.608 1.00 39.27 C N ATOM 1997 CA ASN C 16 34.381 −26.706 −34.469 1.00 35.73 C C ATOM 1998 C ASN C 16 33.650 −25.380 −34.274 1.00 31.63 C C ATOM 1999 O ASN C 16 32.565 −25.346 −33.705 1.00 30.78 C O ATOM 2000 CB ASN C 16 35.103 −27.106 −33.173 1.00 41.02 C C ATOM 2001 CG ASN C 16 34.151 −27.172 −31.964 1.00 49.30 C C ATOM 2002 OD1 ASN C 16 33.053 −27.730 −32.049 1.00 39.61 C O ATOM 2003 ND2 ASN C 16 34.576 −26.601 −30.838 1.00 35.86 C N ATOM 2004 N ARG C 17 34.237 −24.287 −34.745 1.00 19.12 C N ATOM 2005 CA ARG C 17 33.618 −22.985 −34.552 1.00 21.97 C C ATOM 2006 C ARG C 17 32.409 −22.833 −35.466 1.00 23.23 C C ATOM 2007 O ARG C 17 31.385 −22.271 −35.074 1.00 21.76 C O ATOM 2008 CB ARG C 17 34.618 −21.851 −34.783 1.00 18.63 C C ATOM 2009 CG ARG C 17 34.048 −20.470 −34.495 1.00 19.22 C C ATOM 2010 CD ARG C 17 35.129 −19.388 −34.498 1.00 23.09 C C ATOM 2011 NE ARG C 17 35.704 −19.201 −35.826 1.00 26.86 C N ATOM 2012 CZ ARG C 17 36.947 −19.533 −36.164 1.00 30.01 C C ATOM 2013 NH1 ARG C 17 37.775 −20.055 −35.261 1.00 22.90 C N ATOM 2014 NH2 ARG C 17 37.366 −19.328 −37.409 1.00 30.60 C N ATOM 2015 N GLN C 18 32.531 −23.336 −36.687 1.00 26.75 C N ATOM 2016 CA GLN C 18 31.417 −23.314 −37.621 1.00 28.13 C C ATOM 2017 C GLN C 18 30.264 −24.158 −37.079 1.00 24.45 C C ATOM 2018 O GLN C 18 29.106 −23.745 −37.125 1.00 19.76 C O ATOM 2019 CB GLN C 18 31.855 −23.839 −38.990 1.00 24.27 C C ATOM 2020 CG GLN C 18 30.779 −23.713 −40.054 1.00 25.41 C C ATOM 2021 CD GLN C 18 30.429 −22.266 −40.352 1.00 39.70 C C ATOM 2022 OE1 GLN C 18 31.245 −21.517 −40.894 1.00 47.66 C O ATOM 2023 NE2 GLN C 18 29.211 −21.867 −40.004 1.00 49.70 C N ATOM 2024 N VAL C 19 30.603 −25.338 −36.566 1.00 29.15 C N ATOM 2025 CA VAL C 19 29.631 −26.274 −36.016 1.00 28.04 C C ATOM 2026 C VAL C 19 28.932 −25.697 −34.789 1.00 31.99 C C ATOM 2027 O VAL C 19 27.708 −25.733 −34.679 1.00 31.77 C O ATOM 2028 CB VAL C 19 30.314 −27.597 −35.621 1.00 30.57 C C ATOM 2029 CG1 VAL C 19 29.381 −28.459 −34.788 1.00 28.68 C C ATOM 2030 CG2 VAL C 19 30.767 −28.337 −36.856 1.00 28.38 C C ATOM 2031 N THR C 20 29.718 −25.167 −33.863 1.00 23.43 C N ATOM 2032 CA THR C 20 29.167 −24.575 −32.659 1.00 24.62 C C ATOM 2033 C THR C 20 28.283 −23.392 −33.022 1.00 24.14 C C ATOM 2034 O THR C 20 27.247 −23.149 −32.391 1.00 21.70 C O ATOM 2035 CB THR C 20 30.279 −24.114 −31.717 1.00 26.92 C C ATOM 2036 OG1 THR C 20 30.934 −25.264 −31.172 1.00 25.57 C O ATOM 2037 CG2 THR C 20 29.705 −23.271 −30.584 1.00 22.17 C C ATOM 2038 N PHE C 21 28.693 −22.665 −34.053 1.00 21.78 C N ATOM 2039 CA PHE C 21 27.948 −21.492 −34.491 1.00 24.12 C C ATOM 2040 C PHE C 21 26.587 −21.851 −35.081 1.00 23.04 C C ATOM 2041 O PHE C 21 25.603 −21.162 −34.832 1.00 22.41 C O ATOM 2042 CB PHE C 21 28.757 −20.679 −35.501 1.00 19.76 C C ATOM 2043 CG PHE C 21 27.948 −19.642 −36.219 1.00 21.70 C C ATOM 2044 CD1 PHE C 21 27.773 −18.379 −35.672 1.00 16.96 C C ATOM 2045 CD2 PHE C 21 27.349 −19.932 −37.438 1.00 21.89 C C ATOM 2046 CE1 PHE C 21 27.027 −17.419 −36.328 1.00 19.77 C C ATOM 2047 CE2 PHE C 21 26.594 −18.976 −38.100 1.00 22.15 C C ATOM 2048 CZ PHE C 21 26.434 −17.719 −37.549 1.00 26.78 C C ATOM 2049 N THR C 22 26.531 −22.919 −35.869 1.00 17.14 C N ATOM 2050 CA THR C 22 25.265 −23.334 −36.471 1.00 17.72 C C ATOM 2051 C THR C 22 24.301 −23.861 −35.409 1.00 16.28 C C ATOM 2052 O THR C 22 23.096 −23.613 −35.476 1.00 17.19 C O ATOM 2053 CB THR C 22 25.455 −24.402 −37.590 1.00 18.91 C C ATOM 2054 OG1 THR C 22 26.031 −23.796 −38.757 1.00 15.99 C O ATOM 2055 CG2 THR C 22 24.121 −25.011 −37.968 1.00 12.54 C C ATOM 2056 N LYS C 23 24.831 −24.589 −34.428 1.00 18.67 C N ATOM 2057 CA LYS C 23 23.995 −25.125 −33.359 1.00 19.65 C C ATOM 2058 C LYS C 23 23.422 −24.010 −32.493 1.00 19.04 C C ATOM 2059 O LYS C 23 22.209 −23.923 −32.305 1.00 19.52 C O ATOM 2060 CB LYS C 23 24.775 −26.114 −32.488 1.00 22.98 C C ATOM 2061 CG LYS C 23 25.091 −27.443 −33.169 1.00 29.30 C C ATOM 2062 CD LYS C 23 25.900 −28.341 −32.235 1.00 32.52 C C ATOM 2063 CE LYS C 23 26.088 −29.726 −32.813 1.00 35.94 C C ATOM 2064 NZ LYS C 23 27.012 −30.536 −31.973 1.00 33.98 C N ATOM 2065 N ARG C 24 24.302 −23.153 −31.980 1.00 16.23 C N ATOM 2066 CA ARG C 24 23.895 −22.083 −31.072 1.00 15.69 C C ATOM 2067 C ARG C 24 23.079 −20.973 −31.746 1.00 17.54 C C ATOM 2068 O ARG C 24 22.246 −20.339 −31.088 1.00 16.19 C O ATOM 2069 CB ARG C 24 25.106 −21.494 −30.346 1.00 13.13 C C ATOM 2070 CG ARG C 24 25.567 −22.316 −29.145 1.00 14.55 C C ATOM 2071 CD ARG C 24 26.824 −21.735 −28.509 1.00 13.70 C C ATOM 2072 NE ARG C 24 27.168 −22.430 −27.273 1.00 15.96 C N ATOM 2073 CZ ARG C 24 26.860 −21.988 −26.055 1.00 17.74 C C ATOM 2074 NH1 ARG C 24 26.203 −20.842 −25.901 1.00 17.55 C N ATOM 2075 NH2 ARG C 24 27.209 −22.690 −24.990 1.00 13.06 C N ATOM 2076 N LYS C 25 23.313 −20.732 −33.040 1.00 20.57 C N ATOM 2077 CA LYS C 25 22.542 −19.711 −33.763 1.00 21.27 C C ATOM 2078 C LYS C 25 21.087 −20.126 −33.788 1.00 21.17 C C ATOM 2079 O LYS C 25 20.188 −19.314 −33.581 1.00 21.37 C O ATOM 2080 CB LYS C 25 23.040 −19.522 −35.196 1.00 27.14 C C ATOM 2081 CG LYS C 25 22.094 −18.694 −36.068 1.00 23.36 C C ATOM 2082 CD LYS C 25 22.799 −18.097 −37.285 1.00 29.03 C C ATOM 2083 CE LYS C 25 23.198 −19.165 −38.317 1.00 25.05 C C ATOM 2084 NZ LYS C 25 22.025 −19.796 −38.986 1.00 22.30 C N ATOM 2085 N PHE C 26 20.870 −21.407 −34.050 1.00 16.86 C N ATOM 2086 CA PHE C 26 19.541 −21.989 −33.996 1.00 19.25 C C ATOM 2087 C PHE C 26 18.942 −21.777 −32.593 1.00 19.01 C C ATOM 2088 O PHE C 26 17.915 −21.115 −32.435 1.00 20.38 C O ATOM 2089 CB PHE C 26 19.629 −23.478 −34.344 1.00 16.09 C C ATOM 2090 CG PHE C 26 18.300 −24.149 −34.472 1.00 20.27 C C ATOM 2091 CD1 PHE C 26 17.753 −24.395 −35.723 1.00 22.76 C C ATOM 2092 CD2 PHE C 26 17.595 −24.539 −33.343 1.00 18.57 C C ATOM 2093 CE1 PHE C 26 16.525 −25.014 −35.846 1.00 23.64 C C ATOM 2094 CE2 PHE C 26 16.369 −25.160 −33.458 1.00 21.64 C C ATOM 2095 CZ PHE C 26 15.831 −25.398 −34.714 1.00 28.23 C C ATOM 2096 N GLY C 27 19.606 −22.329 −31.579 1.00 21.08 C N ATOM 2097 CA GLY C 27 19.207 −22.147 −30.196 1.00 19.30 C C ATOM 2098 C GLY C 27 18.916 −20.709 −29.804 1.00 17.49 C C ATOM 2099 O GLY C 27 18.010 −20.459 −29.013 1.00 19.26 C O ATOM 2100 N LEU C 28 19.676 −19.760 −30.346 1.00 18.92 C N ATOM 2101 CA LEU C 28 19.486 −18.351 −29.999 1.00 19.41 C C ATOM 2102 C LEU C 28 18.215 −17.781 −30.627 1.00 18.47 C C ATOM 2103 O LEU C 28 17.478 −17.031 −29.983 1.00 16.61 C O ATOM 2104 CB LEU C 28 20.697 −17.513 −30.410 1.00 22.21 C C ATOM 2105 CG LEU C 28 20.668 −16.026 −30.026 1.00 18.79 C C ATOM 2106 CD1 LEU C 28 20.508 −15.853 −28.534 1.00 15.60 C C ATOM 2107 CD2 LEU C 28 21.923 −15.305 −30.508 1.00 16.50 C C ATOM 2108 N MET C 29 17.965 −18.147 −31.883 1.00 24.79 C N ATOM 2109 CA MET C 29 16.753 −17.736 −32.583 1.00 21.90 C C ATOM 2110 C MET C 29 15.530 −18.403 −31.971 1.00 20.00 C C ATOM 2111 O MET C 29 14.478 −17.790 −31.847 1.00 18.56 C O ATOM 2112 CB MET C 29 16.838 −18.074 −34.075 1.00 22.28 C C ATOM 2113 CG MET C 29 17.931 −17.326 −34.839 1.00 21.94 C C ATOM 2114 SD MET C 29 17.603 −17.288 −36.625 1.00 24.71 C S ATOM 2115 CE MET C 29 19.065 −16.419 −37.197 1.00 27.04 C C ATOM 2116 N LYS C 30 15.672 −19.664 −31.585 1.00 18.86 C N ATOM 2117 CA LYS C 30 14.565 −20.375 −30.958 1.00 19.52 C C ATOM 2118 C LYS C 30 14.080 −19.641 −29.701 1.00 19.23 C C ATOM 2119 O LYS C 30 12.881 −19.397 −29.537 1.00 21.59 C O ATOM 2120 CB LYS C 30 14.945 −21.821 −30.627 1.00 18.29 C C ATOM 2121 CG LYS C 30 13.752 −22.660 −30.193 1.00 26.72 C C ATOM 2122 CD LYS C 30 14.138 −24.070 −29.781 1.00 26.48 C C ATOM 2123 CE LYS C 30 12.902 −24.862 −29.372 1.00 33.14 C C ATOM 2124 NZ LYS C 30 13.230 −26.088 −28.587 1.00 28.25 C N ATOM 2125 N LYS C 31 15.010 −19.277 −28.823 1.00 18.87 C N ATOM 2126 CA LYS C 31 14.640 −18.561 −27.600 1.00 22.08 C C ATOM 2127 C LYS C 31 14.141 −17.141 −27.870 1.00 17.64 C C ATOM 2128 O LYS C 31 13.226 −16.662 −27.209 1.00 21.08 C O ATOM 2129 CB LYS C 31 15.790 −18.571 −26.590 1.00 18.89 C C ATOM 2130 CG LYS C 31 15.972 −19.926 −25.938 1.00 20.04 C C ATOM 2131 CD LYS C 31 17.018 −19.903 −24.839 1.00 22.25 C C ATOM 2132 CE LYS C 31 17.024 −21.223 −24.079 1.00 21.58 C C ATOM 2133 NZ LYS C 31 15.661 −21.584 −23.593 1.00 21.26 C N ATOM 2134 N ALA C 32 14.725 −16.476 −28.856 1.00 9.09 C N ATOM 2135 CA ALA C 32 14.263 −15.148 −29.228 1.00 9.04 C C ATOM 2136 C ALA C 32 12.793 −15.201 −29.651 1.00 13.34 C C ATOM 2137 O ALA C 32 11.980 −14.402 −29.184 1.00 13.09 C O ATOM 2138 CB ALA C 32 15.130 −14.569 −30.337 1.00 8.32 C C ATOM 2139 N TYR C 33 12.464 −16.154 −30.524 1.00 19.25 C N ATOM 2140 CA TYR C 33 11.089 −16.391 −30.975 1.00 18.96 C C ATOM 2141 C TYR C 33 10.127 −16.715 −29.822 1.00 21.93 C C ATOM 2142 O TYR C 33 9.026 −16.162 −29.745 1.00 22.45 C O ATOM 2143 CB TYR C 33 11.062 −17.513 −32.026 1.00 23.50 C C ATOM 2144 CG TYR C 33 9.731 −18.234 −32.146 1.00 21.82 C C ATOM 2145 CD1 TYR C 33 8.658 −17.646 −32.804 1.00 26.15 C C ATOM 2146 CD2 TYR C 33 9.551 −19.500 −31.599 1.00 23.49 C C ATOM 2147 CE1 TYR C 33 7.439 −18.297 −32.916 1.00 27.75 C C ATOM 2148 CE2 TYR C 33 8.331 −20.163 −31.700 1.00 23.15 C C ATOM 2149 CZ TYR C 33 7.281 −19.555 −32.362 1.00 29.01 C C ATOM 2150 OH TYR C 33 6.069 −20.198 −32.475 1.00 28.01 C O ATOM 2151 N GLU C 34 10.546 −17.613 −28.934 1.00 21.34 C N ATOM 2152 CA GLU C 34 9.741 −17.988 −27.772 1.00 20.10 C C ATOM 2153 C GLU C 34 9.478 −16.799 −26.852 1.00 20.64 C C ATOM 2154 O GLU C 34 8.376 −16.653 −26.312 1.00 20.34 C O ATOM 2155 CB GLU C 34 10.410 −19.120 −26.989 1.00 19.30 C C ATOM 2156 CG GLU C 34 10.422 −20.458 −27.724 1.00 18.54 C C ATOM 2157 CD GLU C 34 11.121 −21.552 −26.934 1.00 20.08 C C ATOM 2158 OE1 GLU C 34 11.829 −21.227 −25.954 1.00 21.18 C O ATOM 2159 OE2 GLU C 34 10.966 −22.738 −27.292 1.00 17.80 C O ATOM 2160 N LEU C 35 10.485 −15.947 −26.673 1.00 18.35 C N ATOM 2161 CA LEU C 35 10.300 −14.753 −25.852 1.00 18.79 C C ATOM 2162 C LEU C 35 9.309 −13.789 −26.505 1.00 19.94 C C ATOM 2163 O LEU C 35 8.488 −13.171 −25.824 1.00 21.37 C O ATOM 2164 CB LEU C 35 11.627 −14.050 −25.582 1.00 15.90 C C ATOM 2165 CG LEU C 35 11.519 −12.771 −24.750 1.00 18.38 C C ATOM 2166 CD1 LEU C 35 10.931 −13.071 −23.382 1.00 16.74 C C ATOM 2167 CD2 LEU C 35 12.871 −12.089 −24.618 1.00 17.45 C C ATOM 2168 N SER C 36 9.385 −13.661 −27.823 1.00 25.87 C N ATOM 2169 CA SER C 36 8.449 −12.811 −28.548 1.00 31.09 C C ATOM 2170 C SER C 36 6.995 −13.257 −28.326 1.00 28.04 C C ATOM 2171 O SER C 36 6.123 −12.443 −28.038 1.00 29.80 C O ATOM 2172 CB SER C 36 8.778 −12.805 −30.043 1.00 32.46 C C ATOM 2173 OG SER C 36 7.835 −12.024 −30.756 1.00 31.96 C O ATOM 2174 N VAL C 37 6.749 −14.557 −28.450 1.00 20.90 C N ATOM 2175 CA VAL C 37 5.406 −15.109 −28.320 1.00 20.27 C C ATOM 2176 C VAL C 37 4.903 −15.111 −26.873 1.00 22.08 C C ATOM 2177 O VAL C 37 3.773 −14.706 −26.602 1.00 21.87 C O ATOM 2178 CB VAL C 37 5.332 −16.546 −28.876 1.00 21.06 C C ATOM 2179 CG1 VAL C 37 4.025 −17.211 −28.469 1.00 17.91 C C ATOM 2180 CG2 VAL C 37 5.488 −16.541 −30.392 1.00 22.26 C C ATOM 2181 N LEU C 38 5.738 −15.579 −25.952 1.00 28.66 C N ATOM 2182 CA LEU C 38 5.337 −15.712 −24.557 1.00 24.96 C C ATOM 2183 C LEU C 38 4.994 −14.367 −23.933 1.00 26.61 C C ATOM 2184 O LEU C 38 4.017 −14.247 −23.189 1.00 28.76 C O ATOM 2185 CB LEU C 38 6.454 −16.364 −23.739 1.00 24.38 C C ATOM 2186 CG LEU C 38 6.792 −17.832 −23.978 1.00 22.80 C C ATOM 2187 CD1 LEU C 38 8.138 −18.157 −23.352 1.00 20.95 C C ATOM 2188 CD2 LEU C 38 5.703 −18.741 −23.431 1.00 23.41 C C ATOM 2189 N CYS C 39 5.807 −13.359 −24.231 1.00 22.88 C N ATOM 2190 CA CYS C 39 5.695 −12.077 −23.543 1.00 24.78 C C ATOM 2191 C CYS C 39 5.249 −10.941 −24.458 1.00 26.69 C C ATOM 2192 O CYS C 39 5.319 −9.770 −24.089 1.00 30.51 C O ATOM 2193 CB CYS C 39 7.020 −11.733 −22.861 1.00 20.36 C C ATOM 2194 SG CYS C 39 7.564 −13.026 −21.730 1.00 20.08 C S ATOM 2195 N ASP C 40 4.789 −11.294 −25.653 1.00 29.36 C N ATOM 2196 CA ASP C 40 4.248 −10.299 −26.565 1.00 31.01 C C ATOM 2197 C ASP C 40 5.191 −9.102 −26.685 1.00 31.73 C C ATOM 2198 O ASP C 40 4.928 −8.041 −26.125 1.00 30.95 C O ATOM 2199 CB ASP C 40 2.870 −9.845 −26.070 1.00 27.98 C C ATOM 2200 CG ASP C 40 2.188 −8.875 −27.017 1.00 31.87 C C ATOM 2201 OD1 ASP C 40 2.552 −8.826 −28.211 1.00 33.57 C O ATOM 2202 OD2 ASP C 40 1.274 −8.154 −26.559 1.00 47.98 C O ATOM 2203 N CYS C 41 6.298 −9.276 −27.402 1.00 26.23 C N ATOM 2204 CA CYS C 41 7.198 −8.153 −27.658 1.00 31.67 C C ATOM 2205 C CYS C 41 7.834 −8.179 −29.047 1.00 31.20 C C ATOM 2206 O CYS C 41 7.889 −9.224 −29.700 1.00 29.57 C O ATOM 2207 CB CYS C 41 8.264 −8.029 −26.561 1.00 32.05 C C ATOM 2208 SG CYS C 41 8.786 −9.569 −25.798 1.00 39.94 C S ATOM 2209 N GLU C 42 8.279 −7.010 −29.501 1.00 36.27 C N ATOM 2210 CA GLU C 42 9.014 −6.898 −30.751 1.00 32.55 C C ATOM 2211 C GLU C 42 10.475 −7.202 −30.488 1.00 32.26 C C ATOM 2212 O GLU C 42 11.072 −6.659 −29.560 1.00 35.73 C O ATOM 2213 CB GLU C 42 8.912 −5.487 −31.328 1.00 37.23 C C ATOM 2214 CG GLU C 42 7.590 −5.143 −31.974 1.00 51.44 C C ATOM 2215 CD GLU C 42 7.655 −3.824 −32.718 1.00 50.05 C C ATOM 2216 OE1 GLU C 42 6.711 −3.016 −32.585 1.00 70.85 C O ATOM 2217 OE2 GLU C 42 8.658 −3.592 −33.426 1.00 41.10 C O ATOM 2218 N ILE C 43 11.058 −8.056 −31.316 1.00 23.83 C N ATOM 2219 CA ILE C 43 12.456 −8.416 −31.144 1.00 20.13 C C ATOM 2220 C ILE C 43 13.185 −8.409 −32.473 1.00 19.57 C C ATOM 2221 O ILE C 43 12.628 −8.793 −33.498 1.00 20.64 C O ATOM 2222 CB ILE C 43 12.597 −9.788 −30.461 1.00 20.12 C C ATOM 2223 CG1 ILE C 43 12.116 −9.689 −29.009 1.00 20.57 C C ATOM 2224 CG2 ILE C 43 14.038 −10.284 −30.546 1.00 16.02 C C ATOM 2225 CD1 ILE C 43 12.008 −11.011 −28.293 1.00 18.94 C C ATOM 2226 N ALA C 44 14.428 −7.949 −32.454 1.00 23.50 C N ATOM 2227 CA ALA C 44 15.268 −7.984 −33.639 1.00 25.31 C C ATOM 2228 C ALA C 44 16.633 −8.531 −33.268 1.00 24.34 C C ATOM 2229 O ALA C 44 17.238 −8.106 −32.286 1.00 27.29 C O ATOM 2230 CB ALA C 44 15.393 −6.593 −34.259 1.00 22.98 C C ATOM 2231 N LEU C 45 17.115 −9.478 −34.059 1.00 20.02 C N ATOM 2232 CA LEU C 45 18.407 −10.093 −33.815 1.00 17.99 C C ATOM 2233 C LEU C 45 19.197 −10.106 −35.112 1.00 21.52 C C ATOM 2234 O LEU C 45 18.795 −10.747 −36.080 1.00 21.38 C O ATOM 2235 CB LEU C 45 18.217 −11.525 −33.304 1.00 20.52 C C ATOM 2236 CG LEU C 45 19.472 −12.387 −33.136 1.00 21.79 C C ATOM 2237 CD1 LEU C 45 20.440 −11.730 −32.161 1.00 16.43 C C ATOM 2238 CD2 LEU C 45 19.118 −13.805 −32.685 1.00 18.07 C C ATOM 2239 N ILE C 46 20.315 −9.389 −35.133 1.00 23.15 C N ATOM 2240 CA ILE C 46 21.194 −9.369 −36.300 1.00 25.46 C C ATOM 2241 C ILE C 46 22.539 −10.013 −35.976 1.00 25.84 C C ATOM 2242 O ILE C 46 23.200 −9.636 −35.007 1.00 23.37 C O ATOM 2243 CB ILE C 46 21.422 −7.932 −36.808 1.00 28.04 C C ATOM 2244 CG1 ILE C 46 20.168 −7.419 −37.522 1.00 26.67 C C ATOM 2245 CG2 ILE C 46 22.621 −7.884 −37.733 1.00 24.29 C C ATOM 2246 CD1 ILE C 46 20.059 −5.907 −37.569 1.00 26.13 C C ATOM 2247 N ILE C 47 22.937 −10.983 −36.793 1.00 21.24 C N ATOM 2248 CA ILE C 47 24.164 −11.736 −36.563 1.00 21.52 C C ATOM 2249 C ILE C 47 25.027 −11.833 −37.816 1.00 21.63 C C ATOM 2250 O ILE C 47 24.573 −12.316 −38.852 1.00 24.81 C O ATOM 2251 CB ILE C 47 23.857 −13.181 −36.123 1.00 22.08 C C ATOM 2252 CG1 ILE C 47 22.955 −13.203 −34.890 1.00 20.26 C C ATOM 2253 CG2 ILE C 47 25.152 −13.946 −35.860 1.00 22.81 C C ATOM 2254 CD1 ILE C 47 22.536 −14.600 −34.492 1.00 18.30 C C ATOM 2255 N PHE C 48 26.272 −11.384 −37.717 1.00 20.46 C N ATOM 2256 CA PHE C 48 27.259 −11.603 −38.767 1.00 20.03 C C ATOM 2257 C PHE C 48 28.281 −12.567 −38.203 1.00 22.91 C C ATOM 2258 O PHE C 48 28.837 −12.306 −37.143 1.00 26.79 C O ATOM 2259 CB PHE C 48 27.979 −10.300 −39.133 1.00 22.81 C C ATOM 2260 CG PHE C 48 27.063 −9.188 −39.565 1.00 21.27 C C ATOM 2261 CD1 PHE C 48 26.574 −8.277 −38.643 1.00 20.26 C C ATOM 2262 CD2 PHE C 48 26.711 −9.040 −40.899 1.00 25.06 C C ATOM 2263 CE1 PHE C 48 25.737 −7.245 −39.041 1.00 21.07 C C ATOM 2264 CE2 PHE C 48 25.878 −8.009 −41.301 1.00 26.74 C C ATOM 2265 CZ PHE C 48 25.390 −7.111 −40.367 1.00 22.39 C C ATOM 2266 N ASN C 49 28.541 −13.671 −38.893 1.00 26.25 C N ATOM 2267 CA ASN C 49 29.561 −14.607 −38.428 1.00 25.67 C C ATOM 2268 C ASN C 49 30.963 −14.054 −38.686 1.00 26.63 C C ATOM 2269 O ASN C 49 31.107 −12.932 −39.174 1.00 26.67 C O ATOM 2270 CB ASN C 49 29.384 −15.987 −39.070 1.00 23.30 C C ATOM 2271 CG ASN C 49 29.646 −15.976 −40.566 1.00 29.56 C C ATOM 2272 OD1 ASN C 49 30.164 −14.999 −41.118 1.00 29.12 C O ATOM 2273 ND2 ASN C 49 29.288 −17.071 −41.234 1.00 26.62 C N ATOM 2274 N SER C 50 31.989 −14.834 −38.359 1.00 28.75 C N ATOM 2275 CA SER C 50 33.368 −14.384 −38.534 1.00 34.68 C C ATOM 2276 C SER C 50 33.729 −14.177 −40.001 1.00 39.26 C C ATOM 2277 O SER C 50 34.583 −13.354 −40.321 1.00 44.25 C O ATOM 2278 CB SER C 50 34.354 −15.354 −37.872 1.00 34.53 C C ATOM 2279 OG SER C 50 34.054 −16.698 −38.196 1.00 39.66 C O ATOM 2280 N SER C 51 33.076 −14.922 −40.889 1.00 44.85 C N ATOM 2281 CA SER C 51 33.291 −14.765 −42.326 1.00 45.04 C C ATOM 2282 C SER C 51 32.420 −13.647 −42.888 1.00 48.33 C C ATOM 2283 O SER C 51 32.322 −13.478 −44.103 1.00 41.62 C O ATOM 2284 CB SER C 51 33.005 −16.070 −43.066 1.00 39.28 C C ATOM 2285 OG SER C 51 33.839 −17.113 −42.593 1.00 46.61 C O ATOM 2286 N ASN C 52 31.771 −12.911 −41.991 1.00 49.99 C N ATOM 2287 CA ASN C 52 31.033 −11.700 −42.347 1.00 47.32 C C ATOM 2288 C ASN C 52 29.686 −11.923 −43.042 1.00 47.24 C C ATOM 2289 O ASN C 52 29.085 −10.976 −43.552 1.00 47.87 C O ATOM 2290 CB ASN C 52 31.907 −10.776 −43.197 1.00 48.20 C C ATOM 2291 CG ASN C 52 31.878 −9.343 −42.714 1.00 61.86 C C ATOM 2292 OD1 ASN C 52 32.478 −9.010 −41.690 1.00 55.65 C O ATOM 2293 ND2 ASN C 52 31.187 −8.482 −43.453 1.00 61.83 C N ATOM 2294 N LYS C 53 29.210 −13.165 −43.066 1.00 29.68 C N ATOM 2295 CA LYS C 53 27.879 −13.440 −43.605 1.00 33.37 C C ATOM 2296 C LYS C 53 26.774 −13.075 −42.608 1.00 31.12 C C ATOM 2297 O LYS C 53 26.885 −13.342 −41.412 1.00 25.99 C O ATOM 2298 CB LYS C 53 27.735 −14.901 −44.037 1.00 30.60 C C ATOM 2299 CG LYS C 53 26.328 −15.237 −44.537 1.00 38.39 C C ATOM 2300 CD LYS C 53 26.237 −16.650 −45.112 1.00 34.12 C C ATOM 2301 CE LYS C 53 24.811 −16.980 −45.534 1.00 37.02 C C ATOM 2302 NZ LYS C 53 24.680 −18.380 −46.033 1.00 36.06 C N ATOM 2303 N LEU C 54 25.704 −12.475 −43.122 1.00 30.45 C N ATOM 2304 CA LEU C 54 24.601 −11.989 −42.301 1.00 25.57 C C ATOM 2305 C LEU C 54 23.541 −13.053 −41.998 1.00 24.16 C C ATOM 2306 O LEU C 54 23.134 −13.807 −42.875 1.00 32.16 C O ATOM 2307 CB LEU C 54 23.945 −10.794 −42.995 1.00 29.61 C C ATOM 2308 CG LEU C 54 22.636 −10.252 −42.418 1.00 32.79 C C ATOM 2309 CD1 LEU C 54 22.840 −9.712 −41.006 1.00 23.27 C C ATOM 2310 CD2 LEU C 54 22.049 −9.182 −43.336 1.00 28.41 C C ATOM 2311 N PHE C 55 23.103 −13.106 −40.745 1.00 28.59 C N ATOM 2312 CA PHE C 55 21.941 −13.900 −40.355 1.00 28.10 C C ATOM 2313 C PHE C 55 21.018 −13.020 −39.526 1.00 26.52 C C ATOM 2314 O PHE C 55 21.479 −12.122 −38.824 1.00 32.90 C O ATOM 2315 CB PHE C 55 22.358 −15.131 −39.550 1.00 28.39 C C ATOM 2316 CG PHE C 55 23.239 −16.080 −40.307 1.00 23.77 C C ATOM 2317 CD1 PHE C 55 24.614 −15.973 −40.234 1.00 26.43 C C ATOM 2318 CD2 PHE C 55 22.689 −17.081 −41.085 1.00 27.00 C C ATOM 2319 CE1 PHE C 55 25.430 −16.845 −40.927 1.00 31.50 C C ATOM 2320 CE2 PHE C 55 23.496 −17.963 −41.783 1.00 30.53 C C ATOM 2321 CZ PHE C 55 24.869 −17.845 −41.705 1.00 34.41 C C ATOM 2322 N GLN C 56 19.718 −13.263 −39.599 1.00 25.53 C N ATOM 2323 CA GLN C 56 18.785 −12.363 −38.948 1.00 26.25 C C ATOM 2324 C GLN C 56 17.465 −13.010 −38.553 1.00 28.25 C C ATOM 2325 O GLN C 56 17.007 −13.966 −39.181 1.00 30.62 C O ATOM 2326 CB GLN C 56 18.523 −11.149 −39.843 1.00 32.99 C C ATOM 2327 CG GLN C 56 17.979 −11.493 −41.221 1.00 29.99 C C ATOM 2328 CD GLN C 56 17.877 −10.276 −42.131 1.00 41.74 C C ATOM 2329 OE1 GLN C 56 17.110 −9.348 −41.868 1.00 36.88 C O ATOM 2330 NE2 GLN C 56 18.651 −10.279 −43.210 1.00 39.31 C N ATOM 2331 N TYR C 57 16.874 −12.472 −37.491 1.00 20.89 C N ATOM 2332 CA TYR C 57 15.526 −12.814 −37.068 1.00 20.63 C C ATOM 2333 C TYR C 57 14.833 −11.554 −36.575 1.00 22.04 C C ATOM 2334 O TYR C 57 15.459 −10.704 −35.940 1.00 25.74 C O ATOM 2335 CB TYR C 57 15.533 −13.839 −35.929 1.00 25.07 C C ATOM 2336 CG TYR C 57 14.213 −13.867 −35.181 1.00 22.71 C C ATOM 2337 CD1 TYR C 57 13.146 −14.623 −35.644 1.00 21.68 C C ATOM 2338 CD2 TYR C 57 14.020 −13.099 −34.041 1.00 18.82 C C ATOM 2339 CE1 TYR C 57 11.930 −14.635 −34.983 1.00 20.31 C C ATOM 2340 CE2 TYR C 57 12.807 −13.102 −33.369 1.00 18.33 C C ATOM 2341 CZ TYR C 57 11.766 −13.872 −33.844 1.00 22.22 C C ATOM 2342 OH TYR C 57 10.560 −13.885 −33.180 1.00 22.44 C O ATOM 2343 N ALA C 58 13.537 −11.441 −36.852 1.00 20.58 C N ATOM 2344 CA ALA C 58 12.730 −10.359 −36.304 1.00 25.73 C C ATOM 2345 C ALA C 58 11.279 −10.807 −36.148 1.00 24.38 C C ATOM 2346 O ALA C 58 10.775 −11.565 −36.971 1.00 25.44 C O ATOM 2347 CB ALA C 58 12.826 −9.129 −37.178 1.00 26.42 C C ATOM 2348 N SER C 59 10.615 −10.340 −35.091 1.00 22.34 C N ATOM 2349 CA SER C 59 9.232 −10.730 −34.829 1.00 26.18 C C ATOM 2350 C SER C 59 8.270 −10.052 −35.799 1.00 28.25 C C ATOM 2351 O SER C 59 7.095 −10.402 −35.857 1.00 29.20 C O ATOM 2352 CB SER C 59 8.833 −10.444 −33.377 1.00 23.68 C C ATOM 2353 OG SER C 59 9.017 −9.078 −33.047 1.00 22.70 C O ATOM 2354 N THR C 60 8.786 −9.076 −36.547 1.00 41.26 C N ATOM 2355 CA THR C 60 8.072 −8.461 −37.666 1.00 41.75 C C ATOM 2356 C THR C 60 9.098 −8.045 −38.707 1.00 44.36 C C ATOM 2357 O THR C 60 10.258 −8.453 −38.633 1.00 44.49 C O ATOM 2358 CB THR C 60 7.283 −7.209 −37.247 1.00 50.98 C C ATOM 2359 OG1 THR C 60 8.143 −6.318 −36.524 1.00 55.36 C O ATOM 2360 CG2 THR C 60 6.088 −7.582 −36.380 1.00 58.49 C C ATOM 2361 N ASP C 61 8.677 −7.235 −39.674 1.00 33.65 C N ATOM 2362 CA ASP C 61 9.611 −6.694 −40.657 1.00 37.81 C C ATOM 2363 C ASP C 61 10.768 −6.016 −39.933 1.00 38.30 C C ATOM 2364 O ASP C 61 10.559 −5.141 −39.082 1.00 35.38 C O ATOM 2365 CB ASP C 61 8.922 −5.688 −41.585 1.00 39.92 C C ATOM 2366 CG ASP C 61 8.070 −6.356 −42.654 1.00 43.00 C C ATOM 2367 OD1 ASP C 61 7.600 −7.491 −42.434 1.00 44.55 C O ATOM 2368 OD2 ASP C 61 7.865 −5.735 −43.718 1.00 50.00 C O ATOM 2369 N MET C 62 11.987 −6.429 −40.269 1.00 47.81 C N ATOM 2370 CA MET C 62 13.183 −5.871 −39.650 1.00 41.37 C C ATOM 2371 C MET C 62 13.177 −4.343 −39.681 1.00 44.59 C C ATOM 2372 O MET C 62 13.376 −3.695 −38.654 1.00 47.74 C O ATOM 2373 CB MET C 62 14.443 −6.406 −40.332 1.00 33.72 C C ATOM 2374 CG MET C 62 15.737 −5.950 −39.669 1.00 43.23 C C ATOM 2375 SD MET C 62 15.850 −6.454 −37.936 1.00 35.55 C S ATOM 2376 CE MET C 62 16.116 −8.214 −38.110 1.00 32.61 C C ATOM 2377 N ASP C 63 12.938 −3.777 −40.861 1.00 57.74 C N ATOM 2378 CA ASP C 63 12.975 −2.328 −41.044 1.00 58.33 C C ATOM 2379 C ASP C 63 12.066 −1.600 −40.057 1.00 52.55 C C ATOM 2380 O ASP C 63 12.293 −0.434 −39.738 1.00 59.74 C O ATOM 2381 CB ASP C 63 12.592 −1.952 −42.480 1.00 63.84 C C ATOM 2382 CG ASP C 63 11.092 −2.020 −42.723 1.00 75.02 C C ATOM 2383 OD1 ASP C 63 10.476 −0.956 −42.961 1.00 68.03 C O ATOM 2384 OD2 ASP C 63 10.526 −3.134 −42.664 1.00 75.33 C O ATOM 2385 N LYS C 64 11.035 −2.286 −39.578 1.00 39.30 C N ATOM 2386 CA LYS C 64 10.108 −1.681 −38.629 1.00 41.27 C C ATOM 2387 C LYS C 64 10.700 −1.602 −37.220 1.00 43.64 C C ATOM 2388 O LYS C 64 10.672 −0.543 −36.588 1.00 32.45 C O ATOM 2389 CB LYS C 64 8.772 −2.427 −38.623 1.00 39.82 C C ATOM 2390 CG LYS C 64 7.983 −2.266 −39.916 1.00 47.23 C C ATOM 2391 CD LYS C 64 6.671 −3.034 −39.884 1.00 48.40 C C ATOM 2392 CE LYS C 64 5.854 −2.764 −41.138 1.00 49.45 C C ATOM 2393 NZ LYS C 64 4.682 −3.676 −41.241 1.00 56.67 C N ATOM 2394 N VAL C 65 11.242 −2.719 −36.735 1.00 36.46 C N ATOM 2395 CA VAL C 65 11.875 −2.743 −35.421 1.00 33.96 C C ATOM 2396 C VAL C 65 13.000 −1.716 −35.377 1.00 34.08 C C ATOM 2397 O VAL C 65 13.153 −0.983 −34.398 1.00 31.90 C O ATOM 2398 CB VAL C 65 12.461 −4.127 −35.083 1.00 32.40 C C ATOM 2399 CG1 VAL C 65 12.862 −4.181 −33.616 1.00 24.46 C C ATOM 2400 CG2 VAL C 65 11.463 −5.226 −35.406 1.00 30.21 C C ATOM 2401 N LEU C 66 13.783 −1.669 −36.451 1.00 33.80 C N ATOM 2402 CA LEU C 66 14.885 −0.726 −36.546 1.00 34.69 C C ATOM 2403 C LEU C 66 14.385 0.714 −36.476 1.00 43.32 C C ATOM 2404 O LEU C 66 14.915 1.529 −35.717 1.00 40.55 C O ATOM 2405 CB LEU C 66 15.684 −0.958 −37.829 1.00 37.87 C C ATOM 2406 CG LEU C 66 16.467 −2.272 −37.880 1.00 41.36 C C ATOM 2407 CD1 LEU C 66 17.377 −2.307 −39.094 1.00 40.31 C C ATOM 2408 CD2 LEU C 66 17.268 −2.463 −36.599 1.00 34.80 C C ATOM 2409 N LEU C 67 13.358 1.023 −37.258 1.00 41.33 C N ATOM 2410 CA LEU C 67 12.827 2.379 −37.292 1.00 42.27 C C ATOM 2411 C LEU C 67 12.264 2.795 −35.938 1.00 41.27 C C ATOM 2412 O LEU C 67 12.381 3.950 −35.542 1.00 42.99 C O ATOM 2413 CB LEU C 67 11.780 2.530 −38.397 1.00 46.70 C C ATOM 2414 CG LEU C 67 12.391 2.585 −39.802 1.00 55.15 C C ATOM 2415 CD1 LEU C 67 11.316 2.649 −40.878 1.00 59.19 C C ATOM 2416 CD2 LEU C 67 13.357 3.762 −39.926 1.00 49.10 C C ATOM 2417 N LYS C 68 11.664 1.844 −35.230 1.00 31.65 C N ATOM 2418 CA LYS C 68 11.140 2.100 −33.900 1.00 33.17 C C ATOM 2419 C LYS C 68 12.294 2.425 −32.959 1.00 36.81 C C ATOM 2420 O LYS C 68 12.152 3.226 −32.032 1.00 36.59 C O ATOM 2421 CB LYS C 68 10.362 0.882 −33.394 1.00 35.82 C C ATOM 2422 CG LYS C 68 9.523 1.146 −32.148 1.00 38.59 C C ATOM 2423 CD LYS C 68 8.716 −0.082 −31.741 1.00 36.40 C C ATOM 2424 CE LYS C 68 7.671 0.265 −30.686 1.00 34.03 C C ATOM 2425 NZ LYS C 68 6.999 −0.939 −30.118 1.00 38.36 C N ATOM 2426 N TYR C 69 13.442 1.804 −33.212 1.00 40.52 C N ATOM 2427 CA TYR C 69 14.630 2.003 −32.387 1.00 42.48 C C ATOM 2428 C TYR C 69 15.267 3.372 −32.615 1.00 43.40 C C ATOM 2429 O TYR C 69 15.696 4.030 −31.666 1.00 39.36 C O ATOM 2430 CB TYR C 69 15.657 0.900 −32.658 1.00 34.93 C C ATOM 2431 CG TYR C 69 16.992 1.127 −31.984 1.00 29.50 C C ATOM 2432 CD1 TYR C 69 17.206 0.731 −30.671 1.00 30.62 C C ATOM 2433 CD2 TYR C 69 18.037 1.736 −32.662 1.00 31.05 C C ATOM 2434 CE1 TYR C 69 18.423 0.936 −30.055 1.00 26.77 C C ATOM 2435 CE2 TYR C 69 19.258 1.945 −32.053 1.00 28.66 C C ATOM 2436 CZ TYR C 69 19.446 1.543 −30.752 1.00 29.65 C C ATOM 2437 OH TYR C 69 20.664 1.754 −30.143 1.00 31.04 C O ATOM 2438 N THR C 70 15.336 3.791 −33.876 1.00 34.09 C N ATOM 2439 CA THR C 70 15.916 5.086 −34.214 1.00 40.99 C C ATOM 2440 C THR C 70 15.029 6.237 −33.744 1.00 42.40 C C ATOM 2441 O THR C 70 15.524 7.234 −33.212 1.00 46.32 C O ATOM 2442 CB THR C 70 16.226 5.215 −35.726 1.00 38.56 C C ATOM 2443 OG1 THR C 70 15.097 4.777 −36.493 1.00 53.43 C O ATOM 2444 CG2 THR C 70 17.437 4.362 −36.097 1.00 38.86 C C ATOM 2445 N GLU C 71 13.719 6.091 −33.924 1.00 65.54 C N ATOM 2446 CA GLU C 71 12.772 7.104 −33.465 1.00 76.80 C C ATOM 2447 C GLU C 71 12.743 7.167 −31.940 1.00 70.78 C C ATOM 2448 O GLU C 71 12.413 8.200 −31.358 1.00 75.57 C O ATOM 2449 CB GLU C 71 11.359 6.816 −33.992 1.00 72.64 C C ATOM 2450 CG GLU C 71 11.274 6.464 −35.473 1.00 80.52 C C ATOM 2451 CD GLU C 71 11.482 7.652 −36.391 1.00 84.86 C C ATOM 2452 OE1 GLU C 71 11.645 8.782 −35.883 1.00 91.87 C O ATOM 2453 OE2 GLU C 71 11.478 7.453 −37.625 1.00 77.75 C O ATOM 2454 N TYR C 72 13.090 6.054 −31.301 1.00 47.88 C N ATOM 2455 CA TYR C 72 12.996 5.936 −29.849 1.00 46.60 C C ATOM 2456 C TYR C 72 13.701 7.082 −29.129 1.00 43.98 C C ATOM 2457 O TYR C 72 13.248 7.533 −28.074 1.00 41.36 C O ATOM 2458 CB TYR C 72 13.559 4.591 −29.384 1.00 42.97 C C ATOM 2459 CG TYR C 72 13.130 4.183 −27.989 1.00 39.81 C C ATOM 2460 CD1 TYR C 72 11.898 3.577 −27.769 1.00 34.15 C C ATOM 2461 CD2 TYR C 72 13.960 4.398 −26.892 1.00 42.58 C C ATOM 2462 CE1 TYR C 72 11.500 3.195 −26.496 1.00 33.00 C C ATOM 2463 CE2 TYR C 72 13.574 4.019 −25.614 1.00 37.42 C C ATOM 2464 CZ TYR C 72 12.342 3.417 −25.423 1.00 41.04 C C ATOM 2465 OH TYR C 72 11.949 3.037 −24.156 1.00 37.34 C O TER ATOM 2466 N GLY D 2 11.562 −26.613 −16.682 1.00 44.76 D N ATOM 2467 CA GLY D 2 10.788 −26.142 −15.547 1.00 50.33 D C ATOM 2468 C GLY D 2 10.001 −27.255 −14.883 1.00 52.81 D C ATOM 2469 O GLY D 2 10.106 −28.416 −15.283 1.00 48.43 D O ATOM 2470 N ARG D 3 9.213 −26.906 −13.868 1.00 33.83 D N ATOM 2471 CA ARG D 3 8.433 −27.898 −13.132 1.00 35.82 D C ATOM 2472 C ARG D 3 7.466 −28.629 −14.056 1.00 38.35 D C ATOM 2473 O ARG D 3 7.232 −29.830 −13.909 1.00 42.90 D O ATOM 2474 CB ARG D 3 7.679 −27.246 −11.973 1.00 36.26 D C ATOM 2475 CG ARG D 3 8.573 −26.827 −10.813 1.00 38.60 D C ATOM 2476 CD ARG D 3 9.475 −27.974 −10.376 1.00 41.15 D C ATOM 2477 NE ARG D 3 10.365 −27.594 −9.283 1.00 37.71 D N ATOM 2478 CZ ARG D 3 10.010 −27.581 −8.002 1.00 43.27 D C ATOM 2479 NH1 ARG D 3 8.777 −27.919 −7.647 1.00 32.47 D N ATOM 2480 NH2 ARG D 3 10.890 −27.223 −7.076 1.00 42.72 D N ATOM 2481 N LYS D 4 6.907 −27.891 −15.007 1.00 31.39 D N ATOM 2482 CA LYS D 4 6.073 −28.468 −16.048 1.00 31.49 D C ATOM 2483 C LYS D 4 6.503 −27.912 −17.394 1.00 35.40 D C ATOM 2484 O LYS D 4 6.887 −26.745 −17.500 1.00 30.53 D O ATOM 2485 CB LYS D 4 4.598 −28.134 −15.815 1.00 34.27 D C ATOM 2486 CG LYS D 4 3.970 −28.821 −14.615 1.00 38.44 D C ATOM 2487 CD LYS D 4 2.695 −28.101 −14.200 1.00 34.29 D C ATOM 2488 CE LYS D 4 2.224 −28.546 −12.829 1.00 46.09 D C ATOM 2489 NZ LYS D 4 1.259 −27.570 −12.237 1.00 50.05 D N ATOM 2490 N LYS D 5 6.449 −28.751 −18.421 1.00 40.77 D N ATOM 2491 CA LYS D 5 6.620 −28.270 −19.779 1.00 38.60 D C ATOM 2492 C LYS D 5 5.462 −27.339 −20.087 1.00 40.52 D C ATOM 2493 O LYS D 5 4.311 −27.649 −19.774 1.00 41.68 D O ATOM 2494 CB LYS D 5 6.630 −29.431 −20.776 1.00 36.17 D C ATOM 2495 CG LYS D 5 6.437 −28.994 −22.224 1.00 41.05 D C ATOM 2496 CD LYS D 5 6.857 −30.075 −23.210 1.00 37.55 D C ATOM 2497 CE LYS D 5 6.782 −29.563 −24.640 1.00 46.97 D C ATOM 2498 NZ LYS D 5 7.086 −30.620 −25.646 1.00 53.39 D N ATOM 2499 N ILE D 6 5.765 −26.189 −20.678 1.00 41.72 D N ATOM 2500 CA ILE D 6 4.721 −25.288 −21.141 1.00 41.31 D C ATOM 2501 C ILE D 6 4.618 −25.333 −22.655 1.00 47.16 D C ATOM 2502 O ILE D 6 5.421 −25.980 −23.331 1.00 45.51 D O ATOM 2503 CB ILE D 6 4.988 −23.837 −20.726 1.00 45.87 D C ATOM 2504 CG1 ILE D 6 6.267 −23.317 −21.388 1.00 43.98 D C ATOM 2505 CG2 ILE D 6 5.053 −23.716 −19.210 1.00 49.90 D C ATOM 2506 CD1 ILE D 6 6.495 −21.833 −21.180 1.00 41.94 D C ATOM 2507 N GLN D 7 3.617 −24.645 −23.184 1.00 39.50 D N ATOM 2508 CA GLN D 7 3.496 −24.480 −24.619 1.00 40.81 D C ATOM 2509 C GLN D 7 3.747 −23.028 −24.966 1.00 37.12 D C ATOM 2510 O GLN D 7 3.531 −22.138 −24.145 1.00 37.06 D O ATOM 2511 CB GLN D 7 2.122 −24.930 −25.117 1.00 50.71 D C ATOM 2512 CG GLN D 7 2.064 −26.395 −25.528 1.00 48.43 D C ATOM 2513 CD GLN D 7 2.945 −26.703 −26.734 1.00 65.84 D C ATOM 2514 OE1 GLN D 7 3.680 −25.840 −27.223 1.00 69.18 D O ATOM 2515 NE2 GLN D 7 2.870 −27.940 −27.220 1.00 68.00 D N ATOM 2516 N ILE D 8 4.214 −22.794 −26.185 1.00 28.04 D N ATOM 2517 CA ILE D 8 4.606 −21.461 −26.605 1.00 23.21 D C ATOM 2518 C ILE D 8 3.411 −20.664 −27.112 1.00 26.07 D C ATOM 2519 O ILE D 8 3.090 −20.678 −28.299 1.00 25.34 D O ATOM 2520 CB ILE D 8 5.734 −21.519 −27.662 1.00 19.94 D C ATOM 2521 CG1 ILE D 8 6.967 −22.203 −27.066 1.00 20.05 D C ATOM 2522 CG2 ILE D 8 6.100 −20.128 −28.149 1.00 17.49 D C ATOM 2523 CD1 ILE D 8 7.431 −21.586 −25.758 1.00 19.55 D C ATOM 2524 N THR D 9 2.746 −19.978 −26.190 1.00 29.37 D N ATOM 2525 CA THR D 9 1.671 −19.059 −26.540 1.00 29.79 D C ATOM 2526 C THR D 9 1.665 −17.890 −25.555 1.00 26.00 D C ATOM 2527 O THR D 9 2.156 −18.019 −24.433 1.00 29.33 D O ATOM 2528 CB THR D 9 0.297 −19.768 −26.584 1.00 36.05 D C ATOM 2529 OG1 THR D 9 −0.702 −18.862 −27.077 1.00 37.90 D O ATOM 2530 CG2 THR D 9 −0.098 −20.291 −25.203 1.00 27.70 D C ATOM 2531 N ARG D 10 1.130 −16.751 −25.991 1.00 23.06 D N ATOM 2532 CA ARG D 10 1.156 −15.516 −25.206 1.00 27.80 D C ATOM 2533 C ARG D 10 0.578 −15.685 −23.805 1.00 27.06 D C ATOM 2534 O ARG D 10 −0.579 −16.057 −23.644 1.00 29.74 D O ATOM 2535 CB ARG D 10 0.411 −14.401 −25.943 1.00 26.90 D C ATOM 2536 CG ARG D 10 0.455 −13.045 −25.259 1.00 27.50 D C ATOM 2537 CD ARG D 10 −0.540 −12.091 −25.907 1.00 30.44 D C ATOM 2538 NE ARG D 10 −0.591 −10.785 −25.255 1.00 44.07 D N ATOM 2539 CZ ARG D 10 −1.163 −10.559 −24.076 1.00 41.22 D C ATOM 2540 NH1 ARG D 10 −1.722 −11.559 −23.409 1.00 42.54 D N ATOM 2541 NH2 ARG D 10 −1.170 −9.337 −23.559 1.00 34.81 D N ATOM 2542 N ILE D 11 1.400 −15.412 −22.799 1.00 19.71 D N ATOM 2543 CA ILE D 11 0.982 −15.491 −21.405 1.00 20.19 D C ATOM 2544 C ILE D 11 −0.007 −14.372 −21.096 1.00 26.44 D C ATOM 2545 O ILE D 11 0.301 −13.192 −21.265 1.00 24.69 D O ATOM 2546 CB ILE D 11 2.192 −15.388 −20.463 1.00 21.36 D C ATOM 2547 CG1 ILE D 11 3.143 −16.564 −20.704 1.00 16.61 D C ATOM 2548 CG2 ILE D 11 1.740 −15.337 −19.013 1.00 19.56 D C ATOM 2549 CD1 ILE D 11 4.479 −16.424 −20.027 1.00 18.65 D C ATOM 2550 N MET D 12 −1.198 −14.753 −20.651 1.00 27.99 D N ATOM 2551 CA MET D 12 −2.297 −13.806 −20.503 1.00 30.35 D C ATOM 2552 C MET D 12 −2.204 −12.994 −19.216 1.00 36.56 D C ATOM 2553 O MET D 12 −2.780 −11.910 −19.122 1.00 31.16 D O ATOM 2554 CB MET D 12 −3.644 −14.535 −20.576 1.00 30.86 D C ATOM 2555 CG MET D 12 −3.858 −15.321 −21.870 1.00 35.87 D C ATOM 2556 SD MET D 12 −3.790 −14.291 −23.356 1.00 41.14 D S ATOM 2557 CE MET D 12 −5.282 −13.311 −23.140 1.00 28.21 D C ATOM 2558 N ASP D 13 −1.483 −13.521 −18.231 1.00 43.22 D N ATOM 2559 CA ASP D 13 −1.325 −12.844 −16.948 1.00 44.34 D C ATOM 2560 C ASP D 13 −0.190 −11.830 −17.006 1.00 46.62 D C ATOM 2561 O ASP D 13 0.960 −12.195 −17.240 1.00 41.87 D O ATOM 2562 CB ASP D 13 −1.051 −13.860 −15.836 1.00 44.62 D C ATOM 2563 CG ASP D 13 −0.742 −13.200 −14.501 1.00 64.34 D C ATOM 2564 OD1 ASP D 13 −1.403 −12.192 −14.165 1.00 63.68 D O ATOM 2565 OD2 ASP D 13 0.156 −13.692 −13.783 1.00 61.32 D O ATOM 2566 N GLU D 14 −0.517 −10.560 −16.793 1.00 25.49 D N ATOM 2567 CA GLU D 14 0.485 −9.499 −16.775 1.00 27.06 D C ATOM 2568 C GLU D 14 1.566 −9.766 −15.735 1.00 32.28 D C ATOM 2569 O GLU D 14 2.706 −9.342 −15.893 1.00 28.83 D O ATOM 2570 CB GLU D 14 −0.163 −8.142 −16.485 1.00 25.86 D C ATOM 2571 CG GLU D 14 0.825 −6.995 −16.330 1.00 32.28 D C ATOM 2572 CD GLU D 14 0.144 −5.671 −16.005 1.00 57.66 D C ATOM 2573 OE1 GLU D 14 −0.716 −5.641 −15.094 1.00 62.11 D O ATOM 2574 OE2 GLU D 14 0.475 −4.657 −16.659 1.00 50.25 D O ATOM 2575 N ARG D 15 1.208 −10.467 −14.667 1.00 43.07 D N ATOM 2576 CA ARG D 15 2.156 −10.710 −13.590 1.00 36.63 D C ATOM 2577 C ARG D 15 3.201 −11.745 −13.987 1.00 31.76 D C ATOM 2578 O ARG D 15 4.397 −11.465 −13.948 1.00 27.80 D O ATOM 2579 CB ARG D 15 1.435 −11.130 −12.309 1.00 44.69 D C ATOM 2580 CG ARG D 15 2.312 −11.052 −11.080 1.00 50.57 D C ATOM 2581 CD ARG D 15 1.567 −10.443 −9.904 1.00 58.18 D C ATOM 2582 NE ARG D 15 2.426 −9.509 −9.180 1.00 64.06 D N ATOM 2583 CZ ARG D 15 2.457 −8.198 −9.402 1.00 66.22 D C ATOM 2584 NH1 ARG D 15 1.665 −7.659 −10.322 1.00 71.07 D N ATOM 2585 NH2 ARG D 15 3.277 −7.422 −8.702 1.00 44.62 D N ATOM 2586 N ASN D 16 2.748 −12.937 −14.372 1.00 36.62 D N ATOM 2587 CA ASN D 16 3.664 −13.988 −14.798 1.00 31.52 D C ATOM 2588 C ASN D 16 4.335 −13.633 −16.120 1.00 28.43 D C ATOM 2589 O ASN D 16 5.345 −14.225 −16.487 1.00 29.39 D O ATOM 2590 CB ASN D 16 2.957 −15.347 −14.911 1.00 36.44 D C ATOM 2591 CG ASN D 16 3.906 −16.472 −15.369 1.00 46.78 D C ATOM 2592 OD1 ASN D 16 5.005 −16.634 −14.831 1.00 29.58 D O ATOM 2593 ND2 ASN D 16 3.474 −17.251 −16.364 1.00 33.15 D N ATOM 2594 N ARG D 17 3.777 −12.666 −16.838 1.00 20.99 D N ATOM 2595 CA ARG D 17 4.361 −12.290 −18.114 1.00 24.96 D C ATOM 2596 C ARG D 17 5.567 −11.391 −17.900 1.00 26.75 D C ATOM 2597 O ARG D 17 6.542 −11.461 −18.648 1.00 27.52 D O ATOM 2598 CB ARG D 17 3.344 −11.615 −19.034 1.00 23.69 D C ATOM 2599 CG ARG D 17 3.897 −11.348 −20.427 1.00 23.50 D C ATOM 2600 CD ARG D 17 2.832 −10.841 −21.394 1.00 25.68 D C ATOM 2601 NE ARG D 17 2.242 −9.593 −20.931 1.00 32.21 D N ATOM 2602 CZ ARG D 17 0.991 −9.472 −20.502 1.00 33.52 D C ATOM 2603 NH1 ARG D 17 0.179 −10.526 −20.491 1.00 26.29 D N ATOM 2604 NH2 ARG D 17 0.552 −8.290 −20.091 1.00 33.61 D N ATOM 2605 N GLN D 18 5.501 −10.545 −16.878 1.00 32.30 D N ATOM 2606 CA GLN D 18 6.627 −9.685 −16.549 1.00 33.39 D C ATOM 2607 C GLN D 18 7.768 −10.507 −15.957 1.00 28.83 D C ATOM 2608 O GLN D 18 8.935 −10.301 −16.298 1.00 26.19 D O ATOM 2609 CB GLN D 18 6.205 −8.574 −15.583 1.00 32.25 D C ATOM 2610 CG GLN D 18 7.356 −7.676 −15.135 1.00 32.58 D C ATOM 2611 CD GLN D 18 8.132 −7.084 −16.303 1.00 36.60 D C ATOM 2612 OE1 GLN D 18 7.694 −7.142 −17.453 1.00 41.80 D O ATOM 2613 NE2 GLN D 18 9.291 −6.504 −16.008 1.00 46.29 D N ATOM 2614 N VAL D 19 7.415 −11.444 −15.078 1.00 21.98 D N ATOM 2615 CA VAL D 19 8.385 −12.348 −14.470 1.00 25.53 D C ATOM 2616 C VAL D 19 9.081 −13.228 −15.514 1.00 26.27 D C ATOM 2617 O VAL D 19 10.310 −13.331 −15.540 1.00 27.24 D O ATOM 2618 CB VAL D 19 7.719 −13.250 −13.421 1.00 24.87 D C ATOM 2619 CG1 VAL D 19 8.645 −14.396 −13.040 1.00 25.36 D C ATOM 2620 CG2 VAL D 19 7.335 −12.436 −12.203 1.00 28.33 D C ATOM 2621 N THR D 20 8.293 −13.860 −16.376 1.00 28.30 D N ATOM 2622 CA THR D 20 8.858 −14.702 −17.421 1.00 25.46 D C ATOM 2623 C THR D 20 9.730 −13.875 −18.356 1.00 27.14 D C ATOM 2624 O THR D 20 10.819 −14.298 −18.740 1.00 23.40 D O ATOM 2625 CB THR D 20 7.770 −15.430 −18.210 1.00 27.19 D C ATOM 2626 OG1 THR D 20 7.211 −16.461 −17.388 1.00 29.35 D O ATOM 2627 CG2 THR D 20 8.353 −16.058 −19.471 1.00 24.16 D C ATOM 2628 N PHE D 21 9.260 −12.684 −18.703 1.00 21.66 D N ATOM 2629 CA PHE D 21 10.046 −11.782 −19.539 1.00 21.40 D C ATOM 2630 C PHE D 21 11.423 −11.454 −18.939 1.00 18.44 D C ATOM 2631 O PHE D 21 12.421 −11.444 −19.654 1.00 19.17 D O ATOM 2632 CB PHE D 21 9.274 −10.492 −19.831 1.00 18.91 D C ATOM 2633 CG PHE D 21 10.107 −9.427 −20.486 1.00 19.09 D C ATOM 2634 CD1 PHE D 21 10.249 −9.389 −21.862 1.00 16.77 D C ATOM 2635 CD2 PHE D 21 10.753 −8.466 −19.724 1.00 19.35 D C ATOM 2636 CE1 PHE D 21 11.016 −8.413 −22.474 1.00 19.96 D C ATOM 2637 CE2 PHE D 21 11.525 −7.482 −20.327 1.00 21.51 D C ATOM 2638 CZ PHE D 21 11.657 −7.454 −21.703 1.00 27.86 D C ATOM 2639 N THR D 22 11.474 −11.182 −17.638 1.00 21.93 D N ATOM 2640 CA THR D 22 12.739 −10.847 −16.984 1.00 20.58 D C ATOM 2641 C THR D 22 13.703 −12.041 −16.949 1.00 19.47 D C ATOM 2642 O THR D 22 14.895 −11.893 −17.229 1.00 20.26 D O ATOM 2643 CB THR D 22 12.537 −10.271 −15.544 1.00 24.22 D C ATOM 2644 OG1 THR D 22 11.881 −8.995 −15.610 1.00 23.73 D O ATOM 2645 CG2 THR D 22 13.871 −10.089 −14.852 1.00 15.77 D C ATOM 2646 N LYS D 23 13.194 −13.220 −16.607 1.00 17.92 D N ATOM 2647 CA LYS D 23 14.027 −14.418 −16.621 1.00 19.68 D C ATOM 2648 C LYS D 23 14.579 −14.696 −18.021 1.00 18.83 D C ATOM 2649 O LYS D 23 15.793 −14.760 −18.214 1.00 18.51 D O ATOM 2650 CB LYS D 23 13.256 −15.639 −16.108 1.00 21.03 D C ATOM 2651 CG LYS D 23 12.993 −15.645 −14.606 1.00 27.11 D C ATOM 2652 CD LYS D 23 12.078 −16.812 −14.227 1.00 29.06 D C ATOM 2653 CE LYS D 23 11.843 −16.871 −12.728 1.00 28.46 D C ATOM 2654 NZ LYS D 23 10.620 −17.648 −12.375 1.00 33.25 D N ATOM 2655 N ARG D 24 13.685 −14.848 −18.994 1.00 17.07 D N ATOM 2656 CA ARG D 24 14.081 −15.213 −20.359 1.00 17.05 D C ATOM 2657 C ARG D 24 14.898 −14.148 −21.099 1.00 19.13 D C ATOM 2658 O ARG D 24 15.738 −14.494 −21.936 1.00 16.57 D O ATOM 2659 CB ARG D 24 12.868 −15.641 −21.190 1.00 14.08 D C ATOM 2660 CG ARG D 24 12.442 −17.094 −20.962 1.00 15.74 D C ATOM 2661 CD ARG D 24 11.183 −17.438 −21.750 1.00 15.25 D C ATOM 2662 NE ARG D 24 10.793 −18.841 −21.593 1.00 16.71 D N ATOM 2663 CZ ARG D 24 11.206 −19.831 −22.384 1.00 19.10 D C ATOM 2664 NH1 ARG D 24 12.030 −19.590 −23.399 1.00 16.99 D N ATOM 2665 NH2 ARG D 24 10.799 −21.069 −22.159 1.00 17.86 D N ATOM 2666 N LYS D 25 14.673 −12.867 −20.794 1.00 22.27 D N ATOM 2667 CA LYS D 25 15.468 −11.798 −21.413 1.00 22.31 D C ATOM 2668 C LYS D 25 16.932 −11.926 −21.021 1.00 21.68 D C ATOM 2669 O LYS D 25 17.822 −11.822 −21.854 1.00 22.43 D O ATOM 2670 CB LYS D 25 14.962 −10.409 −21.021 1.00 26.53 D C ATOM 2671 CG LYS D 25 15.930 −9.285 −21.404 1.00 22.70 D C ATOM 2672 CD LYS D 25 15.244 −7.918 −21.425 1.00 26.14 D C ATOM 2673 CE LYS D 25 14.832 −7.453 −20.022 1.00 29.54 D C ATOM 2674 NZ LYS D 25 15.996 −7.018 −19.195 1.00 23.97 D N ATOM 2675 N PHE D 26 17.164 −12.143 −19.735 1.00 18.14 D N ATOM 2676 CA PHE D 26 18.496 −12.396 −19.217 1.00 18.95 D C ATOM 2677 C PHE D 26 19.113 −13.614 −19.920 1.00 20.89 D C ATOM 2678 O PHE D 26 20.260 −13.576 −20.362 1.00 22.41 D O ATOM 2679 CB PHE D 26 18.418 −12.620 −17.704 1.00 19.28 D C ATOM 2680 CG PHE D 26 19.745 −12.842 −17.052 1.00 23.11 D C ATOM 2681 CD1 PHE D 26 20.424 −11.786 −16.458 1.00 27.39 D C ATOM 2682 CD2 PHE D 26 20.310 −14.106 −17.015 1.00 20.31 D C ATOM 2683 CE1 PHE D 26 21.653 −11.985 −15.845 1.00 27.22 D C ATOM 2684 CE2 PHE D 26 21.540 −14.313 −16.404 1.00 27.35 D C ATOM 2685 CZ PHE D 26 22.211 −13.250 −15.818 1.00 25.37 D C ATOM 2686 N GLY D 27 18.338 −14.688 −20.029 1.00 26.49 D N ATOM 2687 CA GLY D 27 18.785 −15.895 −20.699 1.00 25.22 D C ATOM 2688 C GLY D 27 19.100 −15.689 −22.168 1.00 24.07 D C ATOM 2689 O GLY D 27 20.000 −16.328 −22.710 1.00 22.92 D O ATOM 2690 N LEU D 28 18.358 −14.800 −22.820 1.00 19.89 D N ATOM 2691 CA LEU D 28 18.568 −14.540 −24.243 1.00 20.40 D C ATOM 2692 C LEU D 28 19.843 −13.731 −24.480 1.00 20.08 D C ATOM 2693 O LEU D 28 20.624 −14.034 −25.380 1.00 17.81 D O ATOM 2694 CB LEU D 28 17.362 −13.822 −24.851 1.00 19.92 D C ATOM 2695 CG LEU D 28 17.417 −13.605 −26.370 1.00 19.33 D C ATOM 2696 CD1 LEU D 28 17.456 −14.923 −27.104 1.00 17.21 D C ATOM 2697 CD2 LEU D 28 16.237 −12.763 −26.841 1.00 18.71 D C ATOM 2698 N MET D 29 20.054 −12.707 −23.659 1.00 23.68 D N ATOM 2699 CA MET D 29 21.264 −11.897 −23.748 1.00 23.30 D C ATOM 2700 C MET D 29 22.492 −12.725 −23.396 1.00 21.30 D C ATOM 2701 O MET D 29 23.542 −12.574 −24.001 1.00 21.35 D O ATOM 2702 CB MET D 29 21.173 −10.677 −22.828 1.00 24.49 D C ATOM 2703 CG MET D 29 20.074 −9.685 −23.197 1.00 24.02 D C ATOM 2704 SD MET D 29 20.345 −8.057 −22.447 1.00 28.67 D S ATOM 2705 CE MET D 29 18.943 −7.151 −23.109 1.00 29.13 D C ATOM 2706 N LYS D 30 22.358 −13.603 −22.411 1.00 20.43 D N ATOM 2707 CA LYS D 30 23.473 −14.454 −22.016 1.00 22.74 D C ATOM 2708 C LYS D 30 23.931 −15.339 −23.180 1.00 21.49 D C ATOM 2709 O LYS D 30 25.126 −15.417 −23.474 1.00 22.26 D O ATOM 2710 CB LYS D 30 23.117 −15.300 −20.791 1.00 22.13 D C ATOM 2711 CG LYS D 30 24.277 −16.134 −20.270 1.00 30.47 D C ATOM 2712 CD LYS D 30 23.915 −16.879 −18.989 1.00 29.56 D C ATOM 2713 CE LYS D 30 25.042 −17.812 −18.567 1.00 31.49 D C ATOM 2714 NZ LYS D 30 24.611 −18.830 −17.568 1.00 32.20 D N ATOM 2715 N LYS D 31 22.983 −15.992 −23.850 1.00 17.89 D N ATOM 2716 CA LYS D 31 23.327 −16.821 −25.010 1.00 19.32 D C ATOM 2717 C LYS D 31 23.835 −16.001 −26.200 1.00 16.48 D C ATOM 2718 O LYS D 31 24.718 −16.442 −26.927 1.00 18.91 D O ATOM 2719 CB LYS D 31 22.169 −17.749 −25.403 1.00 16.34 D C ATOM 2720 CG LYS D 31 22.072 −18.956 −24.485 1.00 15.46 D C ATOM 2721 CD LYS D 31 20.927 −19.876 −24.834 1.00 21.61 D C ATOM 2722 CE LYS D 31 20.909 −21.083 −23.899 1.00 21.65 D C ATOM 2723 NZ LYS D 31 22.219 −21.804 −23.873 1.00 22.50 D N ATOM 2724 N ALA D 32 23.294 −14.801 −26.380 1.00 12.86 D N ATOM 2725 CA ALA D 32 23.778 −13.905 −27.423 1.00 13.63 D C ATOM 2726 C ALA D 32 25.246 −13.545 −27.177 1.00 17.24 D C ATOM 2727 O ALA D 32 26.068 −13.598 −28.097 1.00 15.16 D O ATOM 2728 CB ALA D 32 22.917 −12.649 −27.494 1.00 13.33 D C ATOM 2729 N TYR D 33 25.567 −13.189 −25.931 1.00 20.78 D N ATOM 2730 CA TYR D 33 26.941 −12.884 −25.524 1.00 19.80 D C ATOM 2731 C TYR D 33 27.907 −14.059 −25.734 1.00 21.73 D C ATOM 2732 O TYR D 33 29.020 −13.875 −26.231 1.00 23.12 D O ATOM 2733 CB TYR D 33 26.982 −12.430 −24.053 1.00 25.20 D C ATOM 2734 CG TYR D 33 28.347 −12.555 −23.402 1.00 23.34 D C ATOM 2735 CD1 TYR D 33 29.333 −11.604 −23.627 1.00 25.67 D C ATOM 2736 CD2 TYR D 33 28.649 −13.629 −22.571 1.00 23.73 D C ATOM 2737 CE1 TYR D 33 30.585 −11.713 −23.044 1.00 27.58 D C ATOM 2738 CE2 TYR D 33 29.900 −13.751 −21.983 1.00 23.48 D C ATOM 2739 CZ TYR D 33 30.864 −12.788 −22.223 1.00 27.91 D C ATOM 2740 OH TYR D 33 32.112 −12.893 −21.643 1.00 31.14 D O ATOM 2741 N GLU D 34 27.485 −15.259 −25.344 1.00 16.30 D N ATOM 2742 CA GLU D 34 28.327 −16.447 −25.480 1.00 18.09 D C ATOM 2743 C GLU D 34 28.590 −16.796 −26.940 1.00 19.40 D C ATOM 2744 O GLU D 34 29.687 −17.243 −27.289 1.00 16.16 D O ATOM 2745 CB GLU D 34 27.713 −17.647 −24.749 1.00 16.91 D C ATOM 2746 CG GLU D 34 27.580 −17.446 −23.240 1.00 18.31 D C ATOM 2747 CD GLU D 34 27.022 −18.665 −22.526 1.00 24.07 D C ATOM 2748 OE1 GLU D 34 26.407 −19.524 −23.200 1.00 21.36 D O ATOM 2749 OE2 GLU D 34 27.194 −18.763 −21.291 1.00 19.79 D O ATOM 2750 N LEU D 35 27.594 −16.583 −27.796 1.00 20.14 D N ATOM 2751 CA LEU D 35 27.767 −16.883 −29.216 1.00 19.52 D C ATOM 2752 C LEU D 35 28.752 −15.907 −29.858 1.00 19.84 D C ATOM 2753 O LEU D 35 29.528 −16.279 −30.740 1.00 21.48 D O ATOM 2754 CB LEU D 35 26.432 −16.881 −29.965 1.00 16.57 D C ATOM 2755 CG LEU D 35 26.558 −17.224 −31.453 1.00 17.82 D C ATOM 2756 CD1 LEU D 35 26.909 −18.687 −31.634 1.00 18.16 D C ATOM 2757 CD2 LEU D 35 25.292 −16.887 −32.217 1.00 17.25 D C ATOM 2758 N SER D 36 28.724 −14.660 −29.409 1.00 21.09 D N ATOM 2759 CA SER D 36 29.663 −13.664 −29.913 1.00 30.15 D C ATOM 2760 C SER D 36 31.111 −14.016 −29.541 1.00 25.03 D C ATOM 2761 O SER D 36 32.021 −13.892 −30.356 1.00 27.24 D O ATOM 2762 CB SER D 36 29.302 −12.273 −29.389 1.00 26.99 D C ATOM 2763 OG SER D 36 30.134 −11.289 −29.975 1.00 30.97 D O ATOM 2764 N VAL D 37 31.312 −14.466 −28.308 1.00 20.84 D N ATOM 2765 CA VAL D 37 32.641 −14.814 −27.827 1.00 21.81 D C ATOM 2766 C VAL D 37 33.133 −16.126 −28.435 1.00 22.28 D C ATOM 2767 O VAL D 37 34.225 −16.187 −29.000 1.00 22.33 D O ATOM 2768 CB VAL D 37 32.672 −14.916 −26.286 1.00 21.65 D C ATOM 2769 CG1 VAL D 37 33.953 −15.589 −25.815 1.00 17.21 D C ATOM 2770 CG2 VAL D 37 32.524 −13.535 −25.661 1.00 22.60 D C ATOM 2771 N LEU D 38 32.324 −17.174 −28.313 1.00 26.55 D N ATOM 2772 CA LEU D 38 32.696 −18.493 −28.808 1.00 26.12 D C ATOM 2773 C LEU D 38 33.008 −18.494 −30.302 1.00 26.33 D C ATOM 2774 O LEU D 38 33.987 −19.104 −30.733 1.00 26.16 D O ATOM 2775 CB LEU D 38 31.584 −19.508 −28.529 1.00 24.58 D C ATOM 2776 CG LEU D 38 31.256 −19.849 −27.078 1.00 23.98 D C ATOM 2777 CD1 LEU D 38 29.929 −20.597 −27.006 1.00 20.12 D C ATOM 2778 CD2 LEU D 38 32.379 −20.656 −26.435 1.00 21.85 D C ATOM 2779 N CYS D 39 32.173 −17.822 −31.090 1.00 17.78 D N ATOM 2780 CA CYS D 39 32.296 −17.907 −32.544 1.00 22.24 D C ATOM 2781 C CYS D 39 32.771 −16.616 −33.215 1.00 21.51 D C ATOM 2782 O CYS D 39 32.801 −16.523 −34.442 1.00 24.66 D O ATOM 2783 CB CYS D 39 30.979 −18.382 −33.166 1.00 16.09 D C ATOM 2784 SG CYS D 39 30.384 −19.924 −32.459 1.00 19.92 D S ATOM 2785 N ASP D 40 33.142 −15.623 −32.418 1.00 28.98 D N ATOM 2786 CA ASP D 40 33.704 −14.402 −32.978 1.00 34.97 D C ATOM 2787 C ASP D 40 32.764 −13.804 −34.019 1.00 34.35 D C ATOM 2788 O ASP D 40 33.042 −13.863 −35.217 1.00 31.75 D O ATOM 2789 CB ASP D 40 35.063 −14.706 −33.620 1.00 30.63 D C ATOM 2790 CG ASP D 40 35.796 −13.455 −34.078 1.00 38.54 D C ATOM 2791 OD1 ASP D 40 35.416 −12.338 −33.662 1.00 41.19 D O ATOM 2792 OD2 ASP D 40 36.764 −13.595 −34.859 1.00 49.72 D O ATOM 2793 N CYS D 41 31.652 −13.233 −33.567 1.00 30.83 D N ATOM 2794 CA CYS D 41 30.724 −12.582 −34.485 1.00 35.32 D C ATOM 2795 C CYS D 41 30.102 −11.300 −33.926 1.00 33.52 D C ATOM 2796 O CYS D 41 29.998 −11.126 −32.715 1.00 33.59 D O ATOM 2797 CB CYS D 41 29.642 −13.562 −34.953 1.00 32.70 D C ATOM 2798 SG CYS D 41 29.124 −14.785 −33.747 1.00 41.68 D S ATOM 2799 N GLU D 42 29.723 −10.394 −34.824 1.00 38.03 D N ATOM 2800 CA GLU D 42 29.026 −9.173 −34.443 1.00 39.78 D C ATOM 2801 C GLU D 42 27.562 −9.498 −34.243 1.00 37.32 D C ATOM 2802 O GLU D 42 26.922 −10.070 −35.125 1.00 38.07 D O ATOM 2803 CB GLU D 42 29.129 −8.117 −35.540 1.00 41.70 D C ATOM 2804 CG GLU D 42 30.421 −7.341 −35.586 1.00 51.65 D C ATOM 2805 CD GLU D 42 30.296 −6.100 −36.446 1.00 52.72 D C ATOM 2806 OE1 GLU D 42 31.182 −5.870 −37.294 1.00 69.52 D O ATOM 2807 OE2 GLU D 42 29.301 −5.362 −36.279 1.00 42.59 D O ATOM 2808 N ILE D 43 27.021 −9.121 −33.094 1.00 23.73 D N ATOM 2809 CA ILE D 43 25.625 −9.403 −32.817 1.00 23.65 D C ATOM 2810 C ILE D 43 24.911 −8.176 −32.283 1.00 22.94 D C ATOM 2811 O ILE D 43 25.486 −7.383 −31.541 1.00 24.65 D O ATOM 2812 CB ILE D 43 25.473 −10.568 −31.821 1.00 24.33 D C ATOM 2813 CG1 ILE D 43 26.097 −11.841 −32.402 1.00 21.59 D C ATOM 2814 CG2 ILE D 43 24.006 −10.775 −31.462 1.00 17.28 D C ATOM 2815 CD1 ILE D 43 25.800 −13.090 −31.606 1.00 19.31 D C ATOM 2816 N ALA D 44 23.657 −8.015 −32.686 1.00 19.28 D N ATOM 2817 CA ALA D 44 22.804 −6.973 −32.132 1.00 19.51 D C ATOM 2818 C ALA D 44 21.447 −7.568 −31.789 1.00 17.23 D C ATOM 2819 O ALA D 44 20.908 −8.386 −32.530 1.00 19.16 D O ATOM 2820 CB ALA D 44 22.657 −5.807 −33.109 1.00 17.11 D C ATOM 2821 N LEU D 45 20.906 −7.150 −30.654 1.00 21.67 D N ATOM 2822 CA LEU D 45 19.642 −7.659 −30.167 1.00 18.49 D C ATOM 2823 C LEU D 45 18.854 −6.492 −29.594 1.00 22.56 D C ATOM 2824 O LEU D 45 19.270 −5.884 −28.614 1.00 25.66 D O ATOM 2825 CB LEU D 45 19.902 −8.704 −29.080 1.00 20.89 D C ATOM 2826 CG LEU D 45 18.716 −9.287 −28.309 1.00 21.08 D C ATOM 2827 CD1 LEU D 45 17.745 −9.969 −29.262 1.00 18.48 D C ATOM 2828 CD2 LEU D 45 19.201 −10.255 −27.229 1.00 15.51 D C ATOM 2829 N ILE D 46 17.724 −6.174 −30.215 1.00 30.84 D N ATOM 2830 CA ILE D 46 16.851 −5.107 −29.735 1.00 30.74 D C ATOM 2831 C ILE D 46 15.512 −5.683 −29.296 1.00 30.19 D C ATOM 2832 O ILE D 46 14.876 −6.425 −30.045 1.00 30.65 D O ATOM 2833 CB ILE D 46 16.599 −4.058 −30.832 1.00 32.03 D C ATOM 2834 CG1 ILE D 46 17.889 −3.301 −31.152 1.00 30.14 D C ATOM 2835 CG2 ILE D 46 15.507 −3.098 −30.408 1.00 31.39 D C ATOM 2836 CD1 ILE D 46 17.883 −2.633 −32.510 1.00 33.03 D C ATOM 2837 N ILE D 47 15.084 −5.340 −28.087 1.00 26.87 D N ATOM 2838 CA ILE D 47 13.849 −5.882 −27.528 1.00 24.21 D C ATOM 2839 C ILE D 47 12.950 −4.803 −26.930 1.00 27.15 D C ATOM 2840 O ILE D 47 13.366 −4.063 −26.036 1.00 28.75 D O ATOM 2841 CB ILE D 47 14.146 −6.894 −26.406 1.00 27.99 D C ATOM 2842 CG1 ILE D 47 15.148 −7.952 −26.873 1.00 27.63 D C ATOM 2843 CG2 ILE D 47 12.851 −7.531 −25.900 1.00 30.34 D C ATOM 2844 CD1 ILE D 47 15.679 −8.797 −25.742 1.00 24.42 D C ATOM 2845 N PHE D 48 11.716 −4.726 −27.413 1.00 25.17 D N ATOM 2846 CA PHE D 48 10.718 −3.837 −26.829 1.00 26.76 D C ATOM 2847 C PHE D 48 9.667 −4.690 −26.139 1.00 31.80 D C ATOM 2848 O PHE D 48 8.925 −5.404 −26.806 1.00 30.22 D O ATOM 2849 CB PHE D 48 10.033 −2.993 −27.908 1.00 26.58 D C ATOM 2850 CG PHE D 48 10.962 −2.079 −28.659 1.00 27.99 D C ATOM 2851 CD1 PHE D 48 11.469 −2.448 −29.895 1.00 25.86 D C ATOM 2852 CD2 PHE D 48 11.315 −0.845 −28.136 1.00 29.84 D C ATOM 2853 CE1 PHE D 48 12.320 −1.603 −30.591 1.00 25.17 D C ATOM 2854 CE2 PHE D 48 12.161 0.001 −28.828 1.00 29.95 D C ATOM 2855 CZ PHE D 48 12.664 −0.380 −30.058 1.00 27.12 D C ATOM 2856 N ASN D 49 9.595 −4.619 −24.814 1.00 25.16 D N ATOM 2857 CA ASN D 49 8.601 −5.402 −24.084 1.00 29.35 D C ATOM 2858 C ASN D 49 7.180 −4.950 −24.428 1.00 29.70 D C ATOM 2859 O ASN D 49 6.995 −4.009 −25.201 1.00 30.49 D O ATOM 2860 CB ASN D 49 8.855 −5.348 −22.574 1.00 24.72 D C ATOM 2861 CG ASN D 49 8.473 −4.016 −21.961 1.00 34.53 D C ATOM 2862 OD1 ASN D 49 7.997 −3.108 −22.647 1.00 32.64 D O ATOM 2863 ND2 ASN D 49 8.680 −3.893 −20.654 1.00 26.98 D N ATOM 2864 N SER D 50 6.180 −5.621 −23.866 1.00 32.64 D N ATOM 2865 CA SER D 50 4.789 −5.308 −24.192 1.00 40.15 D C ATOM 2866 C SER D 50 4.389 −3.893 −23.767 1.00 39.76 D C ATOM 2867 O SER D 50 3.391 −3.361 −24.247 1.00 41.34 D O ATOM 2868 CB SER D 50 3.834 −6.344 −23.589 1.00 38.04 D C ATOM 2869 OG SER D 50 3.958 −6.401 −22.179 1.00 41.22 D O ATOM 2870 N SER D 51 5.173 −3.288 −22.876 1.00 39.13 D N ATOM 2871 CA SER D 51 4.925 −1.918 −22.422 1.00 37.74 D C ATOM 2872 C SER D 51 5.769 −0.912 −23.198 1.00 37.71 D C ATOM 2873 O SER D 51 5.913 0.236 −22.777 1.00 28.82 D O ATOM 2874 CB SER D 51 5.226 −1.770 −20.925 1.00 33.74 D C ATOM 2875 OG SER D 51 4.546 −2.747 −20.155 1.00 44.43 D O ATOM 2876 N ASN D 52 6.339 −1.356 −24.316 1.00 43.05 D N ATOM 2877 CA ASN D 52 7.168 −0.503 −25.176 1.00 38.17 D C ATOM 2878 C ASN D 52 8.504 −0.025 −24.602 1.00 37.13 D C ATOM 2879 O ASN D 52 9.169 0.821 −25.202 1.00 38.98 D O ATOM 2880 CB ASN D 52 6.375 0.695 −25.699 1.00 45.39 D C ATOM 2881 CG ASN D 52 5.833 0.463 −27.088 1.00 52.26 D C ATOM 2882 OD1 ASN D 52 5.356 −0.625 −27.404 1.00 42.19 D O ATOM 2883 ND2 ASN D 52 5.909 1.486 −27.933 1.00 50.55 D N ATOM 2884 N LYS D 53 8.902 −0.554 −23.451 1.00 34.11 D N ATOM 2885 CA LYS D 53 10.225 −0.239 −22.920 1.00 35.69 D C ATOM 2886 C LYS D 53 11.318 −0.965 −23.713 1.00 35.71 D C ATOM 2887 O LYS D 53 11.209 −2.158 −23.997 1.00 29.83 D O ATOM 2888 CB LYS D 53 10.326 −0.582 −21.434 1.00 29.99 D C ATOM 2889 CG LYS D 53 11.644 −0.149 −20.803 1.00 38.94 D C ATOM 2890 CD LYS D 53 11.669 −0.437 −19.309 1.00 44.66 D C ATOM 2891 CE LYS D 53 12.963 0.052 −18.674 1.00 37.57 D C ATOM 2892 NZ LYS D 53 13.105 −0.439 −17.277 1.00 38.18 D N ATOM 2893 N LEU D 54 12.368 −0.232 −24.065 1.00 35.22 D N ATOM 2894 CA LEU D 54 13.446 −0.762 −24.889 1.00 29.03 D C ATOM 2895 C LEU D 54 14.521 −1.472 −24.060 1.00 31.24 D C ATOM 2896 O LEU D 54 14.893 −1.012 −22.982 1.00 37.90 D O ATOM 2897 CB LEU D 54 14.073 0.372 −25.704 1.00 33.09 D C ATOM 2898 CG LEU D 54 15.377 0.103 −26.459 1.00 35.38 D C ATOM 2899 CD1 LEU D 54 15.202 −1.013 −27.480 1.00 29.21 D C ATOM 2900 CD2 LEU D 54 15.871 1.375 −27.131 1.00 34.55 D C ATOM 2901 N PHE D 55 15.002 −2.602 −24.568 1.00 25.28 D N ATOM 2902 CA PHE D 55 16.134 −3.308 −23.978 1.00 24.03 D C ATOM 2903 C PHE D 55 17.035 −3.742 −25.115 1.00 22.40 D C ATOM 2904 O PHE D 55 16.551 −4.179 −26.151 1.00 28.76 D O ATOM 2905 CB PHE D 55 15.671 −4.538 −23.196 1.00 24.17 D C ATOM 2906 CG PHE D 55 14.784 −4.220 −22.030 1.00 19.47 D C ATOM 2907 CD1 PHE D 55 13.411 −4.163 −22.185 1.00 18.73 D C ATOM 2908 CD2 PHE D 55 15.325 −3.986 −20.775 1.00 24.11 D C ATOM 2909 CE1 PHE D 55 12.590 −3.873 −21.114 1.00 26.91 D C ATOM 2910 CE2 PHE D 55 14.511 −3.693 −19.691 1.00 22.97 D C ATOM 2911 CZ PHE D 55 13.139 −3.638 −19.861 1.00 29.43 D C ATOM 2912 N GLN D 56 18.343 −3.631 −24.936 1.00 24.35 D N ATOM 2913 CA GLN D 56 19.245 −3.946 −26.028 1.00 23.77 D C ATOM 2914 C GLN D 56 20.546 −4.595 −25.591 1.00 27.79 D C ATOM 2915 O GLN D 56 20.981 −4.452 −24.453 1.00 34.31 D O ATOM 2916 CB GLN D 56 19.540 −2.686 −26.843 1.00 29.59 D C ATOM 2917 CG GLN D 56 20.008 −1.501 −26.014 1.00 28.77 D C ATOM 2918 CD GLN D 56 20.233 −0.254 −26.855 1.00 37.59 D C ATOM 2919 OE1 GLN D 56 20.772 −0.324 −27.961 1.00 36.74 D O ATOM 2920 NE2 GLN D 56 19.821 0.893 −26.332 1.00 35.89 D N ATOM 2921 N TYR D 57 21.151 −5.325 −26.521 1.00 22.60 D N ATOM 2922 CA TYR D 57 22.489 −5.859 −26.355 1.00 23.14 D C ATOM 2923 C TYR D 57 23.214 −5.785 −27.693 1.00 22.80 D C ATOM 2924 O TYR D 57 22.613 −6.004 −28.747 1.00 24.23 D O ATOM 2925 CB TYR D 57 22.468 −7.320 −25.880 1.00 25.34 D C ATOM 2926 CG TYR D 57 23.786 −8.010 −26.165 1.00 23.93 D C ATOM 2927 CD1 TYR D 57 24.880 −7.833 −25.325 1.00 24.98 D C ATOM 2928 CD2 TYR D 57 23.955 −8.790 −27.302 1.00 22.24 D C ATOM 2929 CE1 TYR D 57 26.099 −8.431 −25.594 1.00 23.10 D C ATOM 2930 CE2 TYR D 57 25.170 −9.399 −27.581 1.00 21.19 D C ATOM 2931 CZ TYR D 57 26.240 −9.215 −26.726 1.00 25.96 D C ATOM 2932 OH TYR D 57 27.456 −9.814 −26.997 1.00 20.95 D O ATOM 2933 N ALA D 58 24.508 −5.500 −27.654 1.00 23.20 D N ATOM 2934 CA ALA D 58 25.312 −5.524 −28.866 1.00 25.98 D C ATOM 2935 C ALA D 58 26.761 −5.845 −28.536 1.00 21.59 D C ATOM 2936 O ALA D 58 27.281 −5.390 −27.522 1.00 22.42 D O ATOM 2937 CB ALA D 58 25.204 −4.198 −29.595 1.00 28.83 D C ATOM 2938 N SER D 59 27.409 −6.633 −29.394 1.00 22.61 D N ATOM 2939 CA SER D 59 28.807 −7.013 −29.182 1.00 24.17 D C ATOM 2940 C SER D 59 29.756 −5.829 −29.371 1.00 27.66 D C ATOM 2941 O SER D 59 30.931 −5.913 −29.031 1.00 18.97 D O ATOM 2942 CB SER D 59 29.209 −8.182 −30.087 1.00 20.53 D C ATOM 2943 OG SER D 59 28.979 −7.887 −31.454 1.00 23.14 D O ATOM 2944 N THR D 60 29.237 −4.739 −29.932 1.00 37.48 D N ATOM 2945 CA THR D 60 29.942 −3.461 −29.992 1.00 35.18 D C ATOM 2946 C THR D 60 28.887 −2.370 −29.967 1.00 41.12 D C ATOM 2947 O THR D 60 27.719 −2.643 −29.695 1.00 38.33 D O ATOM 2948 CB THR D 60 30.758 −3.289 −31.282 1.00 43.32 D C ATOM 2949 OG1 THR D 60 29.872 −3.275 −32.409 1.00 45.89 D O ATOM 2950 CG2 THR D 60 31.776 −4.410 −31.444 1.00 53.89 D C ATOM 2951 N ASP D 61 29.287 −1.139 −30.267 1.00 32.58 D N ATOM 2952 CA ASP D 61 28.330 −0.043 −30.326 1.00 31.13 D C ATOM 2953 C ASP D 61 27.159 −0.437 −31.216 1.00 35.70 D C ATOM 2954 O ASP D 61 27.335 −0.752 −32.398 1.00 31.62 D O ATOM 2955 CB ASP D 61 28.983 1.240 −30.845 1.00 36.78 D C ATOM 2956 CG ASP D 61 30.123 1.712 −29.963 1.00 44.94 D C ATOM 2957 OD1 ASP D 61 31.217 1.107 −30.021 1.00 48.90 D O ATOM 2958 OD2 ASP D 61 29.928 2.695 −29.220 1.00 39.72 D O ATOM 2959 N MET D 62 25.967 −0.432 −30.629 1.00 43.29 D N ATOM 2960 CA MET D 62 24.751 −0.809 −31.333 1.00 38.50 D C ATOM 2961 C MET D 62 24.690 −0.227 −32.739 1.00 42.94 D C ATOM 2962 O MET D 62 24.307 −0.909 −33.692 1.00 41.35 D O ATOM 2963 CB MET D 62 23.525 −0.356 −30.545 1.00 31.73 D C ATOM 2964 CG MET D 62 22.224 −0.571 −31.291 1.00 37.28 D C ATOM 2965 SD MET D 62 22.020 −2.280 −31.823 1.00 31.31 D S ATOM 2966 CE MET D 62 21.853 −3.121 −30.255 1.00 24.52 D C ATOM 2967 N ASP D 63 25.074 1.038 −32.861 1.00 46.37 D N ATOM 2968 CA ASP D 63 24.940 1.758 −34.120 1.00 44.58 D C ATOM 2969 C ASP D 63 25.941 1.303 −35.182 1.00 41.10 D C ATOM 2970 O ASP D 63 25.705 1.471 −36.377 1.00 43.44 D O ATOM 2971 CB ASP D 63 25.030 3.263 −33.877 1.00 56.07 D C ATOM 2972 CG ASP D 63 23.875 3.781 −33.033 1.00 63.85 D C ATOM 2973 OD1 ASP D 63 22.752 3.914 −33.570 1.00 56.52 D O ATOM 2974 OD2 ASP D 63 24.089 4.051 −31.830 1.00 64.52 D O ATOM 2975 N LYS D 64 27.051 0.718 −34.750 1.00 39.39 D N ATOM 2976 CA LYS D 64 28.013 0.173 −35.701 1.00 38.16 D C ATOM 2977 C LYS D 64 27.443 −1.065 −36.399 1.00 38.15 D C ATOM 2978 O LYS D 64 27.552 −1.205 −37.618 1.00 31.22 D O ATOM 2979 CB LYS D 64 29.341 −0.148 −35.013 1.00 42.22 D C ATOM 2980 CG LYS D 64 30.070 1.082 −34.497 1.00 52.48 D C ATOM 2981 CD LYS D 64 31.475 0.748 −34.033 1.00 56.05 D C ATOM 2982 CE LYS D 64 32.217 1.996 −33.586 1.00 54.72 D C ATOM 2983 NZ LYS D 64 33.614 1.680 −33.185 1.00 55.86 D N ATOM 2984 N VAL D 65 26.826 −1.952 −35.621 1.00 35.03 D N ATOM 2985 CA VAL D 65 26.206 −3.151 −36.173 1.00 31.99 D C ATOM 2986 C VAL D 65 25.102 −2.778 −37.157 1.00 32.00 D C ATOM 2987 O VAL D 65 24.979 −3.375 −38.230 1.00 28.64 D O ATOM 2988 CB VAL D 65 25.595 −4.036 −35.067 1.00 29.41 D C ATOM 2989 CG1 VAL D 65 25.033 −5.312 −35.664 1.00 24.64 D C ATOM 2990 CG2 VAL D 65 26.630 −4.351 −34.000 1.00 33.52 D C ATOM 2991 N LEU D 66 24.304 −1.782 −36.785 1.00 30.13 D N ATOM 2992 CA LEU D 66 23.175 −1.357 −37.598 1.00 34.53 D C ATOM 2993 C LEU D 66 23.600 −0.784 −38.952 1.00 41.59 D C ATOM 2994 O LEU D 66 23.020 −1.125 −39.985 1.00 39.34 D O ATOM 2995 CB LEU D 66 22.309 −0.363 −36.825 1.00 35.86 D C ATOM 2996 CG LEU D 66 21.616 −0.997 −35.616 1.00 36.70 D C ATOM 2997 CD1 LEU D 66 20.698 −0.009 −34.920 1.00 32.04 D C ATOM 2998 CD2 LEU D 66 20.844 −2.239 −36.046 1.00 31.94 D C ATOM 2999 N LEU D 67 24.615 0.076 −38.950 1.00 45.33 D N ATOM 3000 CA LEU D 67 25.112 0.643 −40.198 1.00 45.57 D C ATOM 3001 C LEU D 67 25.707 −0.442 −41.082 1.00 45.23 D C ATOM 3002 O LEU D 67 25.634 −0.367 −42.306 1.00 48.91 D O ATOM 3003 CB LEU D 67 26.142 1.747 −39.940 1.00 48.90 D C ATOM 3004 CG LEU D 67 25.592 3.174 −39.830 1.00 50.39 D C ATOM 3005 CD1 LEU D 67 24.565 3.429 −40.929 1.00 55.28 D C ATOM 3006 CD2 LEU D 67 24.986 3.442 −38.456 1.00 51.05 D C ATOM 3007 N LYS D 68 26.298 −1.452 −40.455 1.00 30.19 D N ATOM 3008 CA LYS D 68 26.851 −2.574 −41.195 1.00 28.53 D C ATOM 3009 C LYS D 68 25.714 −3.334 −41.864 1.00 36.93 D C ATOM 3010 O LYS D 68 25.860 −3.848 −42.974 1.00 38.76 D O ATOM 3011 CB LYS D 68 27.650 −3.494 −40.269 1.00 31.26 D C ATOM 3012 CG LYS D 68 28.446 −4.569 −41.002 1.00 36.31 D C ATOM 3013 CD LYS D 68 29.462 −5.248 −40.092 1.00 41.17 D C ATOM 3014 CE LYS D 68 30.185 −6.366 −40.824 1.00 38.47 D C ATOM 3015 NZ LYS D 68 31.084 −7.147 −39.930 1.00 37.84 D N ATOM 3016 N TYR D 69 24.574 −3.384 −41.182 1.00 36.80 D N ATOM 3017 CA TYR D 69 23.388 −4.048 −41.711 1.00 38.58 D C ATOM 3018 C TYR D 69 22.826 −3.312 −42.924 1.00 37.48 D C ATOM 3019 O TYR D 69 22.574 −3.916 −43.969 1.00 36.91 D O ATOM 3020 CB TYR D 69 22.312 −4.154 −40.628 1.00 33.48 D C ATOM 3021 CG TYR D 69 20.993 −4.704 −41.125 1.00 28.61 D C ATOM 3022 CD1 TYR D 69 20.791 −6.071 −41.248 1.00 25.44 D C ATOM 3023 CD2 TYR D 69 19.949 −3.856 −41.466 1.00 29.91 D C ATOM 3024 CE1 TYR D 69 19.594 −6.577 −41.694 1.00 23.48 D C ATOM 3025 CE2 TYR D 69 18.743 −4.356 −41.915 1.00 23.47 D C ATOM 3026 CZ TYR D 69 18.573 −5.719 −42.028 1.00 24.70 D C ATOM 3027 OH TYR D 69 17.374 −6.229 −42.478 1.00 27.28 D O ATOM 3028 N THR D 70 22.625 −2.007 −42.779 1.00 35.91 D N ATOM 3029 CA THR D 70 22.044 −1.209 −43.851 1.00 41.72 D C ATOM 3030 C THR D 70 22.985 −1.143 −45.048 1.00 45.23 D C ATOM 3031 O THR D 70 22.556 −1.280 −46.195 1.00 54.00 D O ATOM 3032 CB THR D 70 21.669 0.208 −43.371 1.00 43.34 D C ATOM 3033 OG1 THR D 70 22.794 0.812 −42.723 1.00 52.52 D O ATOM 3034 CG2 THR D 70 20.510 0.140 −42.386 1.00 39.54 D C ATOM 3035 N GLU D 71 24.270 −0.950 −44.775 1.00 37.17 D N ATOM 3036 CA GLU D 71 25.285 −0.959 −45.822 1.00 45.08 D C ATOM 3037 C GLU D 71 25.360 −2.327 −46.502 1.00 40.36 D C ATOM 3038 O GLU D 71 25.728 −2.431 −47.671 1.00 44.26 D O ATOM 3039 CB GLU D 71 26.656 −0.580 −45.247 1.00 34.24 D C ATOM 3040 N TYR D 72 25.014 −3.372 −45.756 1.00 43.08 D N ATOM 3041 CA TYR D 72 25.049 −4.736 −46.269 1.00 44.67 D C ATOM 3042 C TYR D 72 24.000 −4.905 −47.359 1.00 53.17 D C ATOM 3043 O TYR D 72 24.293 −5.401 −48.450 1.00 52.85 D O ATOM 3044 CB TYR D 72 24.790 −5.729 −45.133 1.00 45.47 D C ATOM 3045 CG TYR D 72 25.057 −7.181 −45.473 1.00 41.46 D C ATOM 3046 CD1 TYR D 72 26.211 −7.816 −45.029 1.00 36.92 D C ATOM 3047 CD2 TYR D 72 24.149 −7.922 −46.224 1.00 42.67 D C ATOM 3048 CE1 TYR D 72 26.461 −9.148 −45.328 1.00 34.28 D C ATOM 3049 CE2 TYR D 72 24.386 −9.255 −46.526 1.00 36.45 D C ATOM 3050 CZ TYR D 72 25.542 −9.863 −46.075 1.00 41.64 D C ATOM 3051 OH TYR D 72 25.786 −11.187 −46.372 1.00 43.36 D O ATOM 3052 N ASN D 73 22.775 −4.487 −47.047 1.00 80.06 D N ATOM 3053 CA ASN D 73 21.657 −4.569 −47.981 1.00 81.24 D C ATOM 3054 C ASN D 73 21.840 −3.626 −49.166 1.00 89.74 D C ATOM 3055 O ASN D 73 21.953 −2.411 −48.994 1.00 87.49 D O ATOM 3056 CB ASN D 73 20.332 −4.264 −47.268 1.00 78.13 D C ATOM 3057 CG ASN D 73 19.902 −5.374 −46.315 1.00 68.24 D C ATOM 3058 OD1 ASN D 73 18.773 −5.859 −46.380 1.00 71.72 D O ATOM 3059 ND2 ASN D 73 20.801 −5.778 −45.426 1.00 60.27 D N TER ATOM 3060 O5′ ADE G 1 2.089 −11.162 −3.297 1.00 30.09 G O ATOM 3061 C5′ ADE G 1 1.758 −9.795 −3.078 1.00 31.54 G C ATOM 3062 C4′ ADE G 1 2.994 −8.975 −2.748 1.00 32.18 G C ATOM 3063 O4′ ADE G 1 3.673 −9.553 −1.599 1.00 29.23 G O ATOM 3064 C3′ ADE G 1 4.047 −8.913 −3.851 1.00 36.39 G C ATOM 3065 O3′ ADE G 1 4.751 −7.683 −3.778 1.00 32.25 G O ATOM 3066 C2′ ADE G 1 4.963 −10.064 −3.462 1.00 36.96 G C ATOM 3067 C1′ ADE G 1 5.015 −9.805 −1.964 1.00 31.04 G C ATOM 3068 N9 ADE G 1 5.528 −10.926 −1.189 1.00 30.97 G N ATOM 3069 C8 ADE G 1 6.758 −11.000 −0.601 1.00 31.87 G C ATOM 3070 N7 ADE G 1 6.970 −12.124 0.035 1.00 29.74 G N ATOM 3071 C5 ADE G 1 5.802 −12.836 −0.151 1.00 25.19 G C ATOM 3072 C6 ADE G 1 5.409 −14.110 0.280 1.00 27.04 G C ATOM 3073 N6 ADE G 1 6.195 −14.892 1.021 1.00 29.70 G N ATOM 3074 N1 ADE G 1 4.179 −14.536 −0.076 1.00 33.56 G N ATOM 3075 C2 ADE G 1 3.408 −13.727 −0.818 1.00 33.14 G C ATOM 3076 N3 ADE G 1 3.673 −12.505 −1.284 1.00 29.79 G N ATOM 3077 C4 ADE G 1 4.899 −12.115 −0.907 1.00 29.22 G C ATOM 3078 P ADE G 2 5.814 −7.300 −4.906 1.00 38.84 G P ATOM 3079 OP1 ADE G 2 6.230 −5.901 −4.689 1.00 40.00 G O ATOM 3080 OP2 ADE G 2 5.266 −7.699 −6.218 1.00 34.10 G O ATOM 3081 O5′ ADE G 2 7.049 −8.252 −4.565 1.00 46.24 G O ATOM 3082 C5′ ADE G 2 8.141 −7.809 −3.759 1.00 34.96 G C ATOM 3083 C4′ ADE G 2 9.293 −8.790 −3.905 1.00 37.08 G C ATOM 3084 O4′ ADE G 2 8.859 −10.100 −3.448 1.00 40.16 G O ATOM 3085 C3′ ADE G 2 9.760 −9.022 −5.341 1.00 35.45 G C ATOM 3086 O3′ ADE G 2 11.106 −9.463 −5.356 1.00 43.32 G O ATOM 3087 C2′ ADE G 2 8.863 −10.169 −5.773 1.00 36.55 G C ATOM 3088 C1′ ADE G 2 9.019 −11.013 −4.517 1.00 31.98 G C ATOM 3089 N9 ADE G 2 8.071 −12.116 −4.422 1.00 29.90 G N ATOM 3090 C8 ADE G 2 7.016 −12.377 −5.252 1.00 32.71 G C ATOM 3091 N7 ADE G 2 6.345 −13.460 −4.924 1.00 30.52 G N ATOM 3092 C5 ADE G 2 7.008 −13.937 −3.804 1.00 29.99 G C ATOM 3093 C6 ADE G 2 6.796 −15.056 −2.977 1.00 29.21 G C ATOM 3094 N6 ADE G 2 5.803 −15.932 −3.158 1.00 29.86 G N ATOM 3095 N1 ADE G 2 7.649 −15.243 −1.950 1.00 27.42 G N ATOM 3096 C2 ADE G 2 8.642 −14.369 −1.759 1.00 26.74 G C ATOM 3097 N3 ADE G 2 8.938 −13.282 −2.466 1.00 27.47 G N ATOM 3098 C4 ADE G 2 8.076 −13.122 −3.483 1.00 29.22 G C ATOM 3099 P ADE G 3 12.320 −8.428 −5.459 1.00 41.20 G P ATOM 3100 OP1 ADE G 3 11.995 −7.245 −4.633 1.00 36.86 G O ATOM 3101 OP2 ADE G 3 12.648 −8.262 −6.893 1.00 38.02 G O ATOM 3102 O5′ ADE G 3 13.507 −9.254 −4.767 1.00 33.94 G O ATOM 3103 C5′ ADE G 3 13.430 −9.595 −3.390 1.00 28.55 G C ATOM 3104 C4′ ADE G 3 14.057 −10.954 −3.120 1.00 32.01 G C ATOM 3105 O4′ ADE G 3 13.052 −12.001 −3.180 1.00 29.13 G O ATOM 3106 C3′ ADE G 3 15.169 −11.380 −4.075 1.00 39.18 G C ATOM 3107 O3′ ADE G 3 16.238 −11.933 −3.311 1.00 36.03 G O ATOM 3108 C2′ ADE G 3 14.504 −12.438 −4.960 1.00 33.01 G C ATOM 3109 C1′ ADE G 3 13.501 −13.065 −4.000 1.00 35.72 G C ATOM 3110 N9 ADE G 3 12.333 −13.631 −4.667 1.00 30.02 G N ATOM 3111 C8 ADE G 3 11.696 −13.134 −5.771 1.00 29.04 G C ATOM 3112 N7 ADE G 3 10.663 −13.842 −6.159 1.00 29.82 G N ATOM 3113 C5 ADE G 3 10.618 −14.879 −5.241 1.00 28.28 G C ATOM 3114 C6 ADE G 3 9.747 −15.976 −5.095 1.00 26.79 G C ATOM 3115 N6 ADE G 3 8.719 −16.211 −5.916 1.00 30.72 G N ATOM 3116 N1 ADE G 3 9.980 −16.825 −4.071 1.00 30.91 G N ATOM 3117 C2 ADE G 3 11.013 −16.589 −3.248 1.00 28.20 G C ATOM 3118 N3 ADE G 3 11.893 −15.589 −3.285 1.00 28.13 G N ATOM 3119 C4 ADE G 3 11.639 −14.764 −4.314 1.00 26.77 G C ATOM 3120 P GUA G 4 17.525 −12.572 −4.017 1.00 44.94 G P ATOM 3121 OP1 GUA G 4 18.657 −12.319 −3.104 1.00 26.60 G O ATOM 3122 OP2 GUA G 4 17.569 −12.119 −5.430 1.00 43.10 G O ATOM 3123 O5′ GUA G 4 17.206 −14.141 −4.011 1.00 41.67 G O ATOM 3124 C5′ GUA G 4 17.066 −14.783 −2.751 1.00 41.51 G C ATOM 3125 C4′ GUA G 4 16.533 −16.199 −2.887 1.00 40.62 G C ATOM 3126 O4′ GUA G 4 15.266 −16.214 −3.593 1.00 41.42 G O ATOM 3127 C3′ GUA G 4 17.429 −17.186 −3.627 1.00 49.83 G C ATOM 3128 O3′ GUA G 4 17.570 −18.307 −2.768 1.00 51.67 G O ATOM 3129 C2′ GUA G 4 16.656 −17.515 −4.908 1.00 40.85 G C ATOM 3130 C1′ GUA G 4 15.220 −17.355 −4.420 1.00 36.12 G C ATOM 3131 N9 GUA G 4 14.207 −17.099 −5.442 1.00 35.49 G N ATOM 3132 C8 GUA G 4 14.154 −16.049 −6.329 1.00 31.33 G C ATOM 3133 N7 GUA G 4 13.109 −16.088 −7.115 1.00 30.40 G N ATOM 3134 C5 GUA G 4 12.422 −17.235 −6.723 1.00 31.20 G C ATOM 3135 C6 GUA G 4 11.212 −17.799 −7.209 1.00 29.78 G C ATOM 3136 O6 GUA G 4 10.467 −17.389 −8.120 1.00 26.03 G O ATOM 3137 N1 GUA G 4 10.882 −18.965 −6.518 1.00 27.82 G N ATOM 3138 C2 GUA G 4 11.619 −19.516 −5.497 1.00 32.35 G C ATOM 3139 N2 GUA G 4 11.140 −20.647 −4.957 1.00 36.86 G N ATOM 3140 N3 GUA G 4 12.750 −18.998 −5.034 1.00 30.81 G N ATOM 3141 C4 GUA G 4 13.087 −17.863 −5.691 1.00 32.84 G C ATOM 3142 P CYT G 5 18.538 −19.531 −3.110 1.00 55.72 G P ATOM 3143 OP1 CYT G 5 19.281 −19.838 −1.867 1.00 38.31 G O ATOM 3144 OP2 CYT G 5 19.231 −19.265 −4.393 1.00 40.25 G O ATOM 3145 O5′ CYT G 5 17.491 −20.711 −3.363 1.00 37.47 G O ATOM 3146 C5′ CYT G 5 16.519 −20.951 −2.356 1.00 33.10 G C ATOM 3147 C4′ CYT G 5 15.692 −22.166 −2.706 1.00 33.20 G C ATOM 3148 O4′ CYT G 5 14.748 −21.822 −3.746 1.00 30.86 G O ATOM 3149 C3′ CYT G 5 16.490 −23.358 −3.215 1.00 34.33 G C ATOM 3150 O3′ CYT G 5 15.942 −24.508 −2.587 1.00 39.29 G O ATOM 3151 C2′ CYT G 5 16.264 −23.310 −4.729 1.00 31.29 G C ATOM 3152 C1′ CYT G 5 14.868 −22.703 −4.835 1.00 28.72 G C ATOM 3153 N1 CYT G 5 14.580 −21.859 −6.034 1.00 29.55 G N ATOM 3154 C2 CYT G 5 13.502 −22.187 −6.861 1.00 26.17 G C ATOM 3155 O2 CYT G 5 12.818 −23.189 −6.597 1.00 28.47 G O ATOM 3156 N3 CYT G 5 13.239 −21.397 −7.932 1.00 26.81 G N ATOM 3157 C4 CYT G 5 13.999 −20.328 −8.189 1.00 25.37 G C ATOM 3158 N4 CYT G 5 13.695 −19.590 −9.264 1.00 22.67 G N ATOM 3159 C5 CYT G 5 15.098 −19.973 −7.353 1.00 25.47 G C ATOM 3160 C6 CYT G 5 15.344 −20.758 −6.297 1.00 30.74 G C ATOM 3161 P THY G 6 16.549 −25.968 −2.798 1.00 62.65 G P ATOM 3162 OP1 THY G 6 16.186 −26.778 −1.614 1.00 56.50 G O ATOM 3163 OP2 THY G 6 17.966 −25.841 −3.210 1.00 52.21 G O ATOM 3164 O5′ THY G 6 15.727 −26.497 −4.064 1.00 49.96 G O ATOM 3165 C5′ THY G 6 14.396 −26.977 −3.929 1.00 48.74 G C ATOM 3166 C4′ THY G 6 14.019 −27.782 −5.157 1.00 40.65 G C ATOM 3167 O4′ THY G 6 13.704 −26.874 −6.246 1.00 41.97 G O ATOM 3168 C3′ THY G 6 15.131 −28.676 −5.695 1.00 45.61 G C ATOM 3169 O3′ THY G 6 14.577 −29.772 −6.399 1.00 51.56 G O ATOM 3170 C2′ THY G 6 15.817 −27.746 −6.684 1.00 42.12 G C ATOM 3171 C1′ THY G 6 14.568 −27.158 −7.330 1.00 46.59 G C ATOM 3172 N1 THY G 6 14.811 −25.913 −8.108 1.00 38.83 G N ATOM 3173 C2 THY G 6 13.846 −25.493 −8.994 1.00 36.66 G C ATOM 3174 O2 THY G 6 12.799 −26.093 −9.164 1.00 35.66 G O ATOM 3175 N3 THY G 6 14.152 −24.339 −9.668 1.00 31.51 G N ATOM 3176 C4 THY G 6 15.308 −23.590 −9.545 1.00 33.13 G C ATOM 3177 O4 THY G 6 15.497 −22.569 −10.194 1.00 36.34 G O ATOM 3178 C5 THY G 6 16.280 −24.092 −8.604 1.00 35.08 G C ATOM 3179 C7 THY G 6 17.572 −23.358 −8.395 1.00 29.54 G C ATOM 3180 C6 THY G 6 15.990 −25.217 −7.938 1.00 33.15 G C ATOM 3181 P ADE G 7 14.158 −31.112 −5.635 1.00 45.98 G P ATOM 3182 OP1 ADE G 7 13.536 −30.737 −4.346 1.00 49.15 G O ATOM 3183 OP2 ADE G 7 15.320 −32.024 −5.661 1.00 50.69 G O ATOM 3184 O5′ ADE G 7 13.029 −31.710 −6.594 1.00 37.82 G O ATOM 3185 C5′ ADE G 7 11.731 −31.143 −6.586 1.00 40.93 G C ATOM 3186 C4′ ADE G 7 11.136 −31.093 −7.982 1.00 41.28 G C ATOM 3187 O4′ ADE G 7 11.745 −30.022 −8.750 1.00 42.69 G O ATOM 3188 C3′ ADE G 7 11.307 −32.355 −8.812 1.00 44.26 G C ATOM 3189 O3′ ADE G 7 10.102 −32.546 −9.548 1.00 46.58 G O ATOM 3190 C2′ ADE G 7 12.522 −32.032 −9.691 1.00 39.03 G C ATOM 3191 C1′ ADE G 7 12.369 −30.527 −9.915 1.00 40.77 G C ATOM 3192 N9 ADE G 7 13.605 −29.761 −10.075 1.00 35.79 G N ATOM 3193 C8 ADE G 7 14.800 −29.956 −9.437 1.00 38.83 G C ATOM 3194 N7 ADE G 7 15.733 −29.090 −9.772 1.00 39.23 G N ATOM 3195 C5 ADE G 7 15.106 −28.261 −10.690 1.00 32.85 G C ATOM 3196 C6 ADE G 7 15.548 −27.137 −11.423 1.00 28.85 G C ATOM 3197 N6 ADE G 7 16.783 −26.630 −11.346 1.00 24.36 6 N ATOM 3198 N1 ADE G 7 14.662 −26.547 −12.252 1.00 28.50 G N ATOM 3199 C2 ADE G 7 13.422 −27.042 −12.340 1.00 28.65 G C ATOM 3200 N3 ADE G 7 12.893 −28.087 −11.701 1.00 35.16 G N ATOM 3201 C4 ADE G 7 13.794 −28.659 −10.883 1.00 35.41 G C ATOM 3202 P THY G 8 9.904 −33.839 −10.469 1.00 58.11 G P ATOM 3203 OP1 THY G 8 8.471 −34.212 −10.428 1.00 52.37 G O ATOM 3204 OP2 THY G 8 10.968 −34.817 −10.125 1.00 42.98 G O ATOM 3205 O5′ THY G 8 10.202 −33.255 −11.925 1.00 39.07 G O ATOM 3206 C5′ THY G 8 9.502 −32.094 −12.335 1.00 39.40 G C ATOM 3207 C4′ THY G 8 10.160 −31.489 −13.559 1.00 40.04 G C ATOM 3208 O4′ THY G 8 11.414 −30.863 −13.208 1.00 41.59 G O ATOM 3209 C3′ THY G 8 10.517 −32.477 −14.664 1.00 32.24 G C ATOM 3210 O3′ THY G 8 9.467 −32.466 −15.624 1.00 32.65 G O ATOM 3211 C2′ THY G 8 11.839 −31.938 −15.220 1.00 30.22 G C ATOM 3212 C1′ THY G 8 12.062 −30.645 −14.439 1.00 33.04 G C ATOM 3213 N1 THY G 8 13.493 −30.260 −14.190 1.00 32.43 G N ATOM 3214 C2 THY G 8 14.016 −29.165 −14.847 1.00 30.93 G C ATOM 3215 O2 THY G 8 13.380 −28.485 −15.636 1.00 29.88 G O ATOM 3216 N3 THY G 8 15.327 −28.890 −14.551 1.00 26.98 G N ATOM 3217 C4 THY G 8 16.154 −29.577 −13.683 1.00 29.88 G C ATOM 3218 O4 THY G 8 17.326 −29.246 −13.490 1.00 25.74 G O ATOM 3219 C5 THY G 8 15.541 −30.708 −13.027 1.00 30.10 G C ATOM 3220 C7 THY G 8 16.337 −31.538 −12.060 1.00 38.26 G C ATOM 3221 C6 THY G 8 14.263 −30.992 −13.307 1.00 28.43 G C ATOM 3222 P THY G 9 9.616 −33.145 −17.068 1.00 40.40 G P ATOM 3223 OP1 THY G 9 8.257 −33.380 −17.598 1.00 29.13 G O ATOM 3224 OP2 THY G 9 10.591 −34.251 −16.958 1.00 33.30 G O ATOM 3225 O5′ THY G 9 10.257 −31.979 −17.948 1.00 35.54 G O ATOM 3226 C5′ THY G 9 9.490 −30.803 −18.126 1.00 33.56 G C ATOM 3227 C4′ THY G 9 10.278 −29.781 −18.911 1.00 31.82 G C ATOM 3228 O4′ THY G 9 11.559 −29.580 −18.269 1.00 27.85 G O ATOM 3229 C3′ THY G 9 10.574 −30.170 −20.355 1.00 26.02 G C ATOM 3230 O3′ THY G 9 10.419 −28.984 −21.121 1.00 29.19 G O ATOM 3231 C2′ THY G 9 12.015 −30.683 −20.291 1.00 25.44 G C ATOM 3232 C1′ THY G 9 12.588 −29.753 −19.223 1.00 29.00 G C ATOM 3233 N1 THY G 9 13.781 −30.239 −18.474 1.00 26.11 G N ATOM 3234 C2 THY G 9 14.842 −29.387 −18.366 1.00 23.17 G C ATOM 3235 O2 THY G 9 14.839 −28.276 −18.867 1.00 24.88 G O ATOM 3236 N3 THY G 9 15.901 −29.890 −17.652 1.00 24.78 G N ATOM 3237 C4 THY G 9 16.000 −31.129 −17.047 1.00 22.42 G C ATOM 3238 O4 THY G 9 16.996 −31.492 −16.427 1.00 25.07 G O ATOM 3239 C5 THY G 9 14.851 −31.971 −17.199 1.00 24.19 G C ATOM 3240 C7 THY G 9 14.855 −33.340 −16.582 1.00 24.67 G C ATOM 3241 C6 THY G 9 13.807 −31.492 −17.895 1.00 28.98 G C ATOM 3242 P ADE G 10 10.667 −28.948 −22.697 1.00 27.55 G P ATOM 3243 OP1 ADE G 10 9.807 −27.892 −23.275 1.00 25.17 G O ATOM 3244 OP2 ADE G 10 10.572 −30.334 −23.209 1.00 31.35 G O ATOM 3245 O5′ ADE G 10 12.182 −28.437 −22.773 1.00 37.21 G O ATOM 3246 C5′ ADE G 10 12.484 −27.120 −22.314 1.00 23.68 G C ATOM 3247 C4′ ADE G 10 13.858 −26.640 −22.756 1.00 22.58 G C ATOM 3248 O4′ ADE G 10 14.884 −27.249 −21.939 1.00 22.97 G O ATOM 3249 C3′ ADE G 10 14.259 −26.935 −24.196 1.00 25.44 G C ATOM 3250 O3′ ADE G 10 14.904 −25.776 −24.681 1.00 22.78 G O ATOM 3251 C2′ ADE G 10 15.215 −28.121 −24.073 1.00 18.98 G C ATOM 3252 C1′ ADE G 10 15.893 −27.822 −22.744 1.00 23.52 G C ATOM 3253 N9 ADE G 10 16.359 −28.998 −22.015 1.00 23.49 G N ATOM 3254 C8 ADE G 10 15.649 −30.147 −21.787 1.00 20.29 G C ATOM 3255 N7 ADE G 10 16.309 −31.040 −21.086 1.00 21.42 G N ATOM 3256 C5 ADE G 10 17.529 −30.433 −20.832 1.00 20.13 G C ATOM 3257 C6 ADE G 10 18.673 −30.865 −20.131 1.00 23.13 G C ATOM 3258 N6 ADE G 10 18.761 −32.062 −19.540 1.00 22.41 G N ATOM 3259 N1 ADE G 10 19.723 −30.018 −20.065 1.00 21.54 G N ATOM 3260 C2 ADE G 10 19.626 −28.826 −20.665 1.00 19.94 G C ATOM 3261 N3 ADE G 10 18.602 −28.309 −21.347 1.00 21.70 G N ATOM 3262 C4 ADE G 10 17.577 −29.173 −21.396 1.00 20.19 G C ATOM 3263 P THY G 11 15.529 −25.684 −26.145 1.00 28.15 G P ATOM 3264 OP1 THY G 11 15.315 −24.302 −26.619 1.00 28.86 G O ATOM 3265 OP2 THY G 11 15.080 −26.832 −26.967 1.00 20.38 G O ATOM 3266 O5′ THY G 11 17.085 −25.861 −25.826 1.00 29.02 G O ATOM 3267 C5′ THY G 11 17.711 −24.929 −24.951 1.00 22.15 G C ATOM 3268 C4′ THY G 11 19.189 −25.234 −24.789 1.00 25.89 G C ATOM 3269 O4′ THY G 11 19.351 −26.501 −24.106 1.00 23.80 G O ATOM 3270 C3′ THY G 11 19.983 −25.330 −26.086 1.00 27.91 G C ATOM 3271 O3′ THY G 11 21.157 −24.518 −25.923 1.00 24.16 G O ATOM 3272 C2′ THY G 11 20.256 −26.836 −26.215 1.00 24.53 G C ATOM 3273 C1′ THY G 11 20.358 −27.248 −24.746 1.00 23.90 G C ATOM 3274 N1 THY G 11 20.093 −28.677 −24.366 1.00 21.31 G N ATOM 3275 C2 THY G 11 21.003 −29.314 −23.544 1.00 22.11 G C ATOM 3276 O2 THY G 11 22.023 −28.796 −23.131 1.00 27.11 G O ATOM 3277 N3 THY G 11 20.696 −30.601 −23.208 1.00 20.87 G N ATOM 3278 C4 THY G 11 19.583 −31.305 −23.599 1.00 26.65 G C ATOM 3279 O4 THY G 11 19.404 −32.466 −23.242 1.00 34.71 G O ATOM 3280 C5 THY G 11 18.659 −30.590 −24.453 1.00 22.77 G C ATOM 3281 C7 THY G 11 17.411 −31.282 −24.931 1.00 22.15 G C ATOM 3282 C6 THY G 11 18.948 −29.321 −24.791 1.00 20.01 G C ATOM 3283 P THY G 12 22.165 −24.182 −27.131 1.00 26.73 G P ATOM 3284 OP1 THY G 12 22.786 −22.874 −26.830 1.00 25.84 G O ATOM 3285 OP2 THY G 12 21.475 −24.391 −28.426 1.00 33.91 G O ATOM 3286 O5′ THY G 12 23.291 −25.310 −26.972 1.00 28.10 G O ATOM 3287 C5′ THY G 12 24.116 −25.288 −25.804 1.00 22.77 G C ATOM 3288 C4′ THY G 12 24.934 −26.556 −25.716 1.00 25.11 G C ATOM 3289 O4′ THY G 12 24.081 −27.685 −25.387 1.00 24.96 G O ATOM 3290 C3′ THY G 12 25.642 −26.935 −27.019 1.00 26.10 G C ATOM 3291 O3′ THY G 12 26.982 −27.309 −26.745 1.00 26.65 G O ATOM 3292 C2′ THY G 12 24.836 −28.135 −27.515 1.00 19.97 G C ATOM 3293 C1′ THY G 12 24.544 −28.771 −26.163 1.00 21.80 G C ATOM 3294 N1 THY G 12 23.535 −29.859 −26.186 1.00 22.69 G N ATOM 3295 C2 THY G 12 23.743 −30.974 −25.393 1.00 23.34 G C ATOM 3296 O2 THY G 12 24.706 −31.116 −24.664 1.00 22.76 G O ATOM 3297 N3 THY G 12 22.767 −31.929 −25.484 1.00 20.07 G N ATOM 3298 C4 THY G 12 21.637 −31.872 −26.270 1.00 20.42 G C ATOM 3299 O4 THY G 12 20.824 −32.787 −26.267 1.00 28.04 G O ATOM 3300 C5 THY G 12 21.484 −30.682 −27.080 1.00 19.54 G C ATOM 3301 C7 THY G 12 20.292 −30.510 −27.982 1.00 20.80 G C ATOM 3302 C6 THY G 12 22.431 −29.745 −27.003 1.00 20.75 G C ATOM 3303 P ADE G 13 28.151 −26.224 −26.639 1.00 29.02 G P ATOM 3304 OP1 ADE G 13 27.795 −25.263 −25.568 1.00 26.54 G O ATOM 3305 OP2 ADE G 13 28.443 −25.746 −28.011 1.00 21.47 G O ATOM 3306 O5′ ADE G 13 29.379 −27.113 −26.119 1.00 27.76 G O ATOM 3307 C5′ ADE G 13 29.266 −27.784 −24.858 1.00 24.82 G C ATOM 3308 C4′ ADE G 13 30.220 −28.968 −24.783 1.00 29.40 G C ATOM 3309 O4′ ADE G 13 29.546 −30.226 −25.060 1.00 24.95 G O ATOM 3310 C3′ ADE G 13 31.405 −28.915 −25.739 1.00 22.88 G C ATOM 3311 O3′ ADE G 13 32.510 −29.502 −25.053 1.00 23.06 G O ATOM 3312 C2′ ADE G 13 30.900 −29.716 −26.940 1.00 22.97 G C ATOM 3313 C1′ ADE G 13 29.905 −30.707 −26.338 1.00 26.35 G C ATOM 3314 N9 ADE G 13 28.659 −30.840 −27.083 1.00 21.00 G N ATOM 3315 C8 ADE G 13 28.200 −30.019 −28.074 1.00 18.52 G C ATOM 3316 N7 ADE G 13 27.040 −30.383 −28.562 1.00 19.84 G N ATOM 3317 C5 ADE G 13 26.706 −31.513 −27.834 1.00 17.67 G C ATOM 3318 C6 ADE G 13 25.584 −32.365 −27.868 1.00 18.34 G C ATOM 3319 N6 ADE G 13 24.554 −32.194 −28.711 1.00 17.04 G N ATOM 3320 N1 ADE G 13 25.566 −33.405 −27.004 1.00 19.91 G N ATOM 3321 C2 ADE G 13 26.602 −33.570 −26.170 1.00 19.44 G C ATOM 3322 N3 ADE G 13 27.705 −32.832 −26.046 1.00 18.84 G N ATOM 3323 C4 ADE G 13 27.694 −31.809 −26.915 1.00 19.36 G C ATOM 3324 P GUA G 14 33.898 −29.846 −25.771 1.00 32.65 G P ATOM 3325 OP1 GUA G 14 34.973 −29.788 −24.754 1.00 32.33 G O ATOM 3326 OP2 GUA G 14 33.998 −29.022 −26.998 1.00 23.93 G O ATOM 3327 O5′ GUA G 14 33.703 −31.383 −26.160 1.00 26.41 G O ATOM 3328 C5′ GUA G 14 33.518 −32.312 −25.103 1.00 26.98 G C ATOM 3329 C4′ GUA G 14 33.190 −33.695 −25.629 1.00 35.30 G C ATOM 3330 O4′ GUA G 14 31.894 −33.698 −26.284 1.00 35.26 G O ATOM 3331 C3′ GUA G 14 34.194 −34.247 −26.636 1.00 38.49 G C ATOM 3332 O3′ GUA G 14 34.556 −35.547 −26.198 1.00 42.75 G O ATOM 3333 C2′ GUA G 14 33.433 −34.245 −27.963 1.00 35.46 G C ATOM 3334 C1′ GUA G 14 31.989 −34.402 −27.503 1.00 32.29 G C ATOM 3335 N9 GUA G 14 31.010 −33.838 −28.426 1.00 30.90 G N ATOM 3336 C8 GUA G 14 31.116 −32.675 −29.160 1.00 31.45 G C ATOM 3337 N7 GUA G 14 30.067 −32.428 −29.899 1.00 29.52 G N ATOM 3338 C5 GUA G 14 29.212 −33.493 −29.634 1.00 25.41 G C ATOM 3339 C6 GUA G 14 27.926 −33.776 −30.139 1.00 25.42 G C ATOM 3340 O6 GUA G 14 27.266 −33.118 −30.948 1.00 29.11 G O ATOM 3341 N1 GUA G 14 27.403 −34.958 −29.623 1.00 25.64 G N ATOM 3342 C2 GUA G 14 28.047 −35.770 −28.719 1.00 29.50 G C ATOM 3343 N2 GUA G 14 27.381 −36.867 −28.331 1.00 29.82 G N ATOM 3344 N3 GUA G 14 29.254 −35.516 −28.228 1.00 31.77 G N ATOM 3345 C4 GUA G 14 29.774 −34.368 −28.731 1.00 30.52 G C ATOM 3346 P CYT G 15 35.505 −36.506 −27.051 1.00 54.28 G P ATOM 3347 OP1 CYT G 15 36.447 −37.139 −26.101 1.00 62.73 G O ATOM 3348 OP2 CYT G 15 36.014 −35.772 −28.233 1.00 47.29 G O ATOM 3349 O5′ CYT G 15 34.460 −37.607 −27.548 1.00 52.63 G O ATOM 3350 C5′ CYT G 15 33.573 −38.181 −26.592 1.00 53.62 G C ATOM 3351 C4′ CYT G 15 32.470 −38.966 −27.277 1.00 58.86 G C ATOM 3352 O4′ CYT G 15 31.601 −38.072 −28.021 1.00 51.47 G O ATOM 3353 C3′ CYT G 15 32.956 −40.011 −28.277 1.00 61.10 G C ATOM 3354 O3′ CYT G 15 32.168 −41.184 −28.119 1.00 67.43 G O ATOM 3355 C2′ CYT G 15 32.728 −39.339 −29.630 1.00 50.29 G C ATOM 3356 C1′ CYT G 15 31.450 −38.562 −29.339 1.00 46.79 G C ATOM 3357 N1 CYT G 15 31.213 −37.403 −30.243 1.00 40.11 G N ATOM 3358 C2 CYT G 15 30.017 −37.344 −30.967 1.00 34.63 G C ATOM 3359 O2 CYT G 15 29.188 −38.259 −30.840 1.00 36.27 G O ATOM 3360 N3 CYT G 15 29.803 −36.280 −31.785 1.00 29.35 G N ATOM 3361 C4 CYT G 15 30.722 −35.316 −31.891 1.00 33.10 G C ATOM 3362 N4 CYT G 15 30.454 −34.295 −32.714 1.00 30.61 G N ATOM 3363 C5 CYT G 15 31.949 −35.363 −31.159 1.00 34.90 G C ATOM 3364 C6 CYT G 15 32.148 −36.413 −30.354 1.00 36.04 G C ATOM 3365 P THY G 16 32.672 −42.606 −28.657 1.00 78.68 G P ATOM 3366 OP1 THY G 16 32.518 −43.562 −27.536 1.00 50.64 G O ATOM 3367 OP2 THY G 16 33.979 −42.435 −29.342 1.00 63.43 G O ATOM 3368 O5′ THY G 16 31.590 −42.950 −29.783 1.00 70.30 G O ATOM 3369 C5′ THY G 16 30.199 −42.830 −29.506 1.00 65.85 G C ATOM 3370 C4′ THY G 16 29.414 −43.044 −30.786 1.00 64.65 G C ATOM 3371 O4′ THY G 16 29.315 −41.810 −31.544 1.00 56.89 G O ATOM 3372 C3′ THY G 16 30.042 −44.062 −31.730 1.00 65.14 G C ATOM 3373 O3′ THY G 16 29.007 −44.854 −32.288 1.00 70.25 G O ATOM 3374 C2′ THY G 16 30.740 −43.188 −32.771 1.00 55.68 G C ATOM 3375 C1′ THY G 16 29.732 −42.051 −32.873 1.00 50.22 G C ATOM 3376 N1 THY G 16 30.256 −40.770 −33.414 1.00 47.13 G N ATOM 3377 C2 THY G 16 29.417 −40.015 −34.201 1.00 41.96 G C ATOM 3378 O2 THY G 16 28.279 −40.363 −34.473 1.00 36.49 G O ATOM 3379 N3 THY G 16 29.965 −38.839 −34.656 1.00 36.69 G N ATOM 3380 C4 THY G 16 31.240 −38.363 −34.403 1.00 38.39 G C ATOM 3381 O4 THY G 16 31.654 −37.296 −34.849 1.00 36.45 G O ATOM 3382 C5 THY G 16 32.061 −39.205 −33.574 1.00 39.77 G C ATOM 3383 C7 THY G 16 33.458 −38.768 −33.250 1.00 36.90 G C ATOM 3384 C6 THY G 16 31.541 −40.355 −33.119 1.00 43.68 G C ATOM 3385 P THY G 17 29.304 −46.363 −32.712 1.00 77.32 G P ATOM 3386 OP1 THY G 17 28.327 −47.238 −32.024 1.00 59.40 G O ATOM 3387 OP2 THY G 17 30.758 −46.597 −32.559 1.00 72.89 G O ATOM 3388 O5′ THY G 17 28.986 −46.342 −34.277 1.00 72.58 G O ATOM 3389 C5′ THY G 17 27.648 −46.174 −34.735 1.00 67.07 G C ATOM 3390 C4′ THY G 17 27.670 −45.705 −36.178 1.00 67.99 G C ATOM 3391 O4′ THY G 17 28.227 −44.366 −36.227 1.00 63.26 G O ATOM 3392 C3′ THY G 17 28.524 −46.566 −37.110 1.00 64.72 G C ATOM 3393 O3′ THY G 17 27.805 −46.864 −38.302 1.00 70.10 G O ATOM 3394 C2′ THY G 17 29.749 −45.700 −37.392 1.00 64.86 G C ATOM 3395 C1′ THY G 17 29.155 −44.302 −37.283 1.00 70.81 G C ATOM 3396 N1 THY G 17 30.165 −43.280 −36.948 1.00 61.92 G N ATOM 3397 C2 THY G 17 29.971 −41.973 −37.348 1.00 54.43 G C ATOM 3398 O2 THY G 17 28.988 −41.597 −37.970 1.00 42.14 G O ATOM 3399 N3 THY G 17 30.982 −41.118 −36.981 1.00 43.42 G N ATOM 3400 C4 THY G 17 32.130 −41.437 −36.279 1.00 45.64 G C ATOM 3401 O4 THY G 17 32.978 −40.598 −36.002 1.00 48.61 G O ATOM 3402 C5 THY G 17 32.264 −42.821 −35.897 1.00 61.56 G C ATOM 3403 C7 THY G 17 33.471 −43.283 −35.133 1.00 68.79 G C ATOM 3404 C6 THY G 17 31.288 −43.667 −36.248 1.00 58.84 G C TER ATOM 3405 O5′ THY H 1 35.925 −36.030 −41.955 1.00 32.94 H O ATOM 3406 C5′ THY H 1 36.090 −35.750 −43.338 1.00 26.10 H C ATOM 3407 C4′ THY H 1 34.748 −35.736 −44.051 1.00 24.93 H C ATOM 3408 O4′ THY H 1 34.124 −37.044 −43.969 1.00 26.72 H O ATOM 3409 C3′ THY H 1 33.737 −34.740 −43.496 1.00 26.47 H C ATOM 3410 O3′ THY H 1 33.035 −34.134 −44.575 1.00 27.28 H O ATOM 3411 C2′ THY H 1 32.837 −35.598 −42.606 1.00 30.24 H C ATOM 3412 C1′ THY H 1 32.898 −36.976 −43.266 1.00 26.52 H C ATOM 3413 N1 THY H 1 32.836 −38.138 −42.310 1.00 25.05 H N ATOM 3414 C2 THY H 1 31.673 −38.878 −42.229 1.00 24.12 H C ATOM 3415 O2 THY H 1 30.678 −38.651 −42.891 1.00 29.79 H O ATOM 3416 N3 THY H 1 31.702 −39.913 −41.338 1.00 21.97 H N ATOM 3417 C4 THY H 1 32.752 −40.277 −40.528 1.00 24.78 H C ATOM 3418 O4 THY H 1 32.673 −41.229 −39.761 1.00 30.41 H O ATOM 3419 C5 THY H 1 33.938 −39.466 −40.649 1.00 23.79 H C ATOM 3420 C7 THY H 1 35.133 −39.787 −39.804 1.00 30.54 H C ATOM 3421 C6 THY H 1 33.930 −38.445 −41.520 1.00 24.66 H C ATOM 3422 P ADE H 2 32.281 −32.738 −44.373 1.00 39.81 H P ATOM 3423 OP1 ADE H 2 32.238 −32.023 −45.662 1.00 40.11 H O ATOM 3424 OP2 ADE H 2 32.845 −32.071 −43.182 1.00 31.36 H O ATOM 3425 O5′ ADE H 2 30.800 −33.199 −44.012 1.00 38.96 H O ATOM 3426 C5′ ADE H 2 30.137 −34.174 −44.793 1.00 26.70 H C ATOM 3427 C4′ ADE H 2 28.912 −34.646 −44.031 1.00 33.63 H C ATOM 3428 O4′ ADE H 2 29.305 −35.527 −42.943 1.00 38.83 H O ATOM 3429 C3′ ADE H 2 28.096 −33.540 −43.370 1.00 35.55 H C ATOM 3430 O3′ ADE H 2 26.752 −33.943 −43.445 1.00 42.10 H O ATOM 3431 C2′ ADE H 2 28.613 −33.534 −41.931 1.00 30.13 H C ATOM 3432 C1′ ADE H 2 28.809 −35.029 −41.713 1.00 30.36 H C ATOM 3433 N9 ADE H 2 29.756 −35.402 −40.663 1.00 26.40 H N ATOM 3434 C8 ADE H 2 30.726 −34.630 −40.086 1.00 28.73 H C ATOM 3435 N7 ADE H 2 31.427 −35.260 −39.165 1.00 28.81 H N ATOM 3436 C5 ADE H 2 30.880 −36.532 −39.142 1.00 26.92 H C ATOM 3437 C6 ADE H 2 31.167 −37.686 −38.387 1.00 25.71 H C ATOM 3438 N6 ADE H 2 32.131 −37.739 −37.469 1.00 28.67 H N ATOM 3439 N1 ADE H 2 30.426 −38.793 −38.610 1.00 25.67 H N ATOM 3440 C2 ADE H 2 29.461 −38.747 −39.531 1.00 24.75 H C ATOM 3441 N3 ADE H 2 29.102 −37.723 −40.302 1.00 26.66 H N ATOM 3442 C4 ADE H 2 29.853 −36.636 −40.060 1.00 27.31 H C ATOM 3443 P ADE H 3 25.537 −32.924 −43.269 1.00 37.68 H P ATOM 3444 OP1 ADE H 3 25.052 −32.573 −44.625 1.00 39.11 H O ATOM 3445 OP2 ADE H 3 25.908 −31.868 −42.298 1.00 36.68 H O ATOM 3446 O5′ ADE H 3 24.475 −33.891 −42.568 1.00 30.66 H O ATOM 3447 C5′ ADE H 3 24.342 −35.214 −43.063 1.00 30.61 H C ATOM 3448 C4′ ADE H 3 23.861 −36.132 −41.960 1.00 27.07 H C ATOM 3449 O4′ ADE H 3 24.945 −36.425 −41.041 1.00 27.15 H O ATOM 3450 C3′ ADE H 3 22.734 −35.546 −41.114 1.00 38.17 H C ATOM 3451 O3′ ADE H 3 21.727 −36.533 −40.943 1.00 35.18 H O ATOM 3452 C2′ ADE H 3 23.406 −35.175 −39.787 1.00 31.35 H C ATOM 3453 C1′ ADE H 3 24.503 −36.233 −39.709 1.00 34.45 H C ATOM 3454 N9 ADE H 3 25.666 −35.869 −38.903 1.00 26.51 H N ATOM 3455 C8 ADE H 3 26.333 −34.673 −38.872 1.00 28.15 H C ATOM 3456 N7 ADE H 3 27.358 −34.655 −38.047 1.00 28.07 H N ATOM 3457 C5 ADE H 3 27.364 −35.933 −37.502 1.00 27.87 H C ATOM 3458 C6 ADE H 3 28.197 −36.572 −36.559 1.00 24.49 H C ATOM 3459 N6 ADE H 3 29.238 −35.984 −35.964 1.00 28.81 H N ATOM 3460 N1 ADE H 3 27.912 −37.853 −36.241 1.00 27.07 H N ATOM 3461 C2 ADE H 3 26.869 −38.458 −36.826 1.00 26.59 H C ATOM 3462 N3 ADE H 3 26.022 −37.964 −37.727 1.00 28.66 H N ATOM 3463 C4 ADE H 3 26.325 −36.690 −38.022 1.00 28.33 H C ATOM 3464 P GUA H 4 20.373 −36.128 −40.204 1.00 38.36 H P ATOM 3465 OP1 GUA H 4 19.287 −36.963 −40.758 1.00 32.04 H O ATOM 3466 OP2 GUA H 4 20.290 −34.647 −40.237 1.00 39.60 H O ATOM 3467 O5′ GUA H 4 20.659 −36.603 −38.696 1.00 40.06 H O ATOM 3468 C5′ GUA H 4 20.817 −38.005 −38.466 1.00 36.35 H C ATOM 3469 C4′ GUA H 4 21.469 −38.332 −37.131 1.00 39.32 H C ATOM 3470 O4′ GUA H 4 22.664 −37.542 −36.913 1.00 41.95 H O ATOM 3471 C3′ GUA H 4 20.607 −38.121 −35.888 1.00 50.29 H C ATOM 3472 O3′ GUA H 4 20.415 −39.409 −35.314 1.00 52.14 H O ATOM 3473 C2′ GUA H 4 21.433 −37.180 −35.000 1.00 39.71 H C ATOM 3474 C1′ GUA H 4 22.845 −37.449 −35.516 1.00 37.91 H C ATOM 3475 N9 GUA H 4 23.873 −36.430 −35.285 1.00 34.32 H N ATOM 3476 C8 GUA H 4 23.917 −35.163 −35.816 1.00 32.75 H C ATOM 3477 N7 GUA H 4 24.967 −34.480 −35.455 1.00 32.33 H N ATOM 3478 C5 GUA H 4 25.678 −35.349 −34.635 1.00 32.09 H C ATOM 3479 C6 GUA H 4 26.908 −35.161 −33.949 1.00 29.46 H C ATOM 3480 O6 GUA H 4 27.644 −34.161 −33.920 1.00 27.01 H O ATOM 3481 N1 GUA H 4 27.269 −36.298 −33.234 1.00 30.36 H N ATOM 3482 C2 GUA H 4 26.540 −37.459 −33.182 1.00 33.51 H C ATOM 3483 N2 GUA H 4 27.060 −38.439 −32.431 1.00 38.20 H N ATOM 3484 N3 GUA H 4 25.387 −37.649 −33.815 1.00 32.09 H N ATOM 3485 C4 GUA H 4 25.018 −36.555 −34.524 1.00 33.22 H C ATOM 3486 P CYT H 5 19.453 −39.649 −34.057 1.00 55.11 H P ATOM 3487 OP1 CYT H 5 18.684 −40.887 −34.324 1.00 35.30 H O ATOM 3488 OP2 CYT H 5 18.767 −38.374 −33.738 1.00 41.73 H O ATOM 3489 O5′ CYT H 5 20.505 −39.951 −32.890 1.00 44.98 H O ATOM 3490 C5′ CYT H 5 21.501 −40.935 −33.116 1.00 36.84 H C ATOM 3491 C4′ CYT H 5 22.377 −41.096 −31.890 1.00 34.69 H C ATOM 3492 O4′ CYT H 5 23.328 −40.005 −31.777 1.00 30.60 H O ATOM 3493 C3′ CYT H 5 21.623 −41.133 −30.569 1.00 32.70 H C ATOM 3494 O3′ CYT H 5 22.280 −42.089 −29.765 1.00 38.87 H O ATOM 3495 C2′ CYT H 5 21.779 −39.706 −30.040 1.00 29.93 H C ATOM 3496 C1′ CYT H 5 23.178 −39.355 −30.530 1.00 30.85 H C ATOM 3497 N1 CYT H 5 23.446 −37.923 −30.818 1.00 32.57 H N ATOM 3498 C2 CYT H 5 24.513 −37.289 −30.181 1.00 28.31 H C ATOM 3499 O2 CYT H 5 25.194 −37.930 −29.371 1.00 30.53 H O ATOM 3500 N3 CYT H 5 24.771 −35.990 −30.466 1.00 29.17 H N ATOM 3501 C4 CYT H 5 24.015 −35.331 −31.345 1.00 28.71 H C ATOM 3502 N4 CYT H 5 24.319 −34.049 −31.580 1.00 26.57 H N ATOM 3503 C5 CYT H 5 22.920 −35.958 −32.012 1.00 26.39 H C ATOM 3504 C6 CYT H 5 22.679 −37.244 −31.724 1.00 34.07 H C ATOM 3505 P THY H 6 21.626 −42.654 −28.425 1.00 47.41 H P ATOM 3506 OP1 THY H 6 22.066 −44.059 −28.267 1.00 51.76 H O ATOM 3507 OP2 THY H 6 20.184 −42.310 −28.415 1.00 50.29 H O ATOM 3508 O5′ THY H 6 22.348 −41.762 −27.313 1.00 46.65 H O ATOM 3509 C5′ THY H 6 23.725 −41.957 −27.019 1.00 43.24 H C ATOM 3510 C4′ THY H 6 24.116 −41.139 −25.804 1.00 39.41 H C ATOM 3511 O4′ THY H 6 24.396 −39.776 −26.215 1.00 42.16 H O ATOM 3512 C3′ THY H 6 23.026 −41.017 −24.750 1.00 40.48 H C ATOM 3513 O3′ THY H 6 23.617 −40.802 −23.485 1.00 46.66 H O ATOM 3514 C2′ THY H 6 22.315 −39.745 −25.192 1.00 41.24 H C ATOM 3515 C1′ THY H 6 23.550 −38.906 −25.486 1.00 42.05 H C ATOM 3516 N1 THY H 6 23.298 −37.688 −26.293 1.00 34.71 H N ATOM 3517 C2 THY H 6 24.259 −36.704 −26.309 1.00 34.93 H C ATOM 3518 O2 THY H 6 25.305 −36.793 −25.692 1.00 37.85 H O ATOM 3519 N3 THY H 6 23.951 −35.612 −27.080 1.00 31.24 H N ATOM 3520 C4 THY H 6 22.797 −35.421 −27.816 1.00 31.75 H C ATOM 3521 O4 THY H 6 22.607 −34.408 −28.479 1.00 30.53 H O ATOM 3522 C5 THY H 6 21.830 −36.489 −27.749 1.00 32.63 H C ATOM 3523 C7 THY H 6 20.538 −36.385 −28.507 1.00 28.89 H C ATOM 3524 C6 THY H 6 22.122 −37.560 −27.000 1.00 31.00 H C ATOM 3525 P ADE H 7 23.900 −42.022 −22.497 1.00 44.28 H P ATOM 3526 OP1 ADE H 7 24.428 −43.144 −23.303 1.00 40.56 H O ATOM 3527 OP2 ADE H 7 22.691 −42.211 −21.665 1.00 44.27 H O ATOM 3528 O5′ ADE H 7 25.065 −41.436 −21.569 1.00 32.81 H O ATOM 3529 C5′ ADE H 7 26.365 −41.293 −22.115 1.00 32.80 H C ATOM 3530 C4′ ADE H 7 27.031 −40.015 −21.640 1.00 35.14 H C ATOM 3531 O4′ ADE H 7 26.448 −38.855 −22.294 1.00 37.44 H O ATOM 3532 C3′ ADE H 7 26.918 −39.744 −20.149 1.00 38.41 H C ATOM 3533 O3′ ADE H 7 28.144 −39.153 −19.715 1.00 38.15 H O ATOM 3534 C2′ ADE H 7 25.717 −38.794 −20.060 1.00 35.26 H C ATOM 3535 C1′ ADE H 7 25.863 −37.980 −21.345 1.00 37.50 H C ATOM 3536 N9 ADE H 7 24.621 −37.499 −21.953 1.00 30.16 H N ATOM 3537 C8 ADE H 7 23.424 −38.156 −22.049 1.00 32.36 H C ATOM 3538 N7 ADE H 7 22.490 −37.470 −22.674 1.00 33.29 H N ATOM 3539 C5 ADE H 7 23.119 −36.283 −23.023 1.00 27.61 H C ATOM 3540 C6 ADE H 7 22.680 −35.129 −23.709 1.00 23.15 H C ATOM 3541 N6 ADE H 7 21.441 −34.976 −24.190 1.00 21.35 H N ATOM 3542 N1 ADE H 7 23.570 −34.127 −23.879 1.00 23.18 H N ATOM 3543 C2 ADE H 7 24.810 −34.274 −23.404 1.00 24.54 H C ATOM 3544 N3 ADE H 7 25.341 −35.308 −22.749 1.00 29.70 H N ATOM 3545 C4 ADE H 7 24.435 −36.289 −22.588 1.00 31.92 H C ATOM 3546 P ADE H 8 28.347 −38.809 −18.169 1.00 58.35 H P ATOM 3547 OP1 ADE H 8 29.786 −38.970 −17.855 1.00 45.52 H O ATOM 3548 OP2 ADE H 8 27.304 −39.547 −17.411 1.00 40.27 H O ATOM 3549 O5′ ADE H 8 27.993 −37.253 −18.109 1.00 41.83 H O ATOM 3550 C5′ ADE H 8 28.734 −36.350 −18.906 1.00 41.53 H C ATOM 3551 C4′ ADE H 8 28.065 −34.991 −18.913 1.00 43.43 H C ATOM 3552 O4′ ADE H 8 26.830 −35.073 −19.655 1.00 44.70 H O ATOM 3553 C3′ ADE H 8 27.682 −34.434 −17.544 1.00 38.12 H C ATOM 3554 O3′ ADE H 8 28.599 −33.402 −17.223 1.00 36.90 H O ATOM 3555 C2′ ADE H 8 26.262 −33.896 −17.724 1.00 35.36 H C ATOM 3556 C1′ ADE H 8 26.032 −33.996 −19.228 1.00 37.49 H C ATOM 3557 N9 ADE H 8 24.652 −34.286 −19.603 1.00 36.04 H N ATOM 3558 C8 ADE H 8 23.938 −35.416 −19.312 1.00 35.51 H C ATOM 3559 N7 ADE H 8 22.715 −35.408 −19.784 1.00 34.40 H N ATOM 3560 C5 ADE H 8 22.625 −34.186 −20.427 1.00 31.66 H C ATOM 3561 C6 ADE H 8 21.576 −33.572 −21.130 1.00 36.96 H C ATOM 3562 N6 ADE H 8 20.385 −34.157 −21.290 1.00 32.17 H N ATOM 3563 N1 ADE H 8 21.802 −32.347 −21.657 1.00 34.88 H N ATOM 3564 C2 ADE H 8 23.006 −31.781 −21.483 1.00 38.52 H C ATOM 3565 N3 ADE H 8 24.074 −32.262 −20.837 1.00 32.76 H N ATOM 3566 C4 ADE H 8 23.809 −33.480 −20.330 1.00 33.22 H C ATOM 3567 P THY H 9 28.397 −32.411 −15.982 1.00 36.15 H P ATOM 3568 OP1 THY H 9 29.753 −32.044 −15.512 1.00 28.93 H O ATOM 3569 OP2 THY H 9 27.402 −32.984 −15.044 1.00 34.70 H O ATOM 3570 O5′ THY H 9 27.768 −31.124 −16.688 1.00 32.97 H O ATOM 3571 C5′ THY H 9 28.548 −30.497 −17.690 1.00 33.48 H C ATOM 3572 C4′ THY H 9 27.801 −29.333 −18.307 1.00 31.92 H C ATOM 3573 O4′ THY H 9 26.530 −29.798 −18.818 1.00 25.84 H O ATOM 3574 C3′ THY H 9 27.493 −28.172 −17.365 1.00 26.38 H C ATOM 3575 O3′ THY H 9 27.716 −26.976 −18.100 1.00 25.95 H O ATOM 3576 C2′ THY H 9 26.025 −28.395 −16.999 1.00 24.26 H C ATOM 3577 C1′ THY H 9 25.491 −29.001 −18.293 1.00 25.25 H C ATOM 3578 N1 THY H 9 24.315 −29.902 −18.168 1.00 23.43 H N ATOM 3579 C2 THY H 9 23.279 −29.705 −19.043 1.00 25.36 H C ATOM 3580 O2 THY H 9 23.298 −28.825 −19.883 1.00 27.24 H O ATOM 3581 N3 THY H 9 22.230 −30.577 −18.888 1.00 26.75 H N ATOM 3582 C4 THY H 9 22.123 −31.604 −17.968 1.00 24.08 H C ATOM 3583 O4 THY H 9 21.143 −32.337 −17.900 1.00 25.41 H O ATOM 3584 C5 THY H 9 23.243 −31.757 −17.084 1.00 25.32 H C ATOM 3585 C7 THY H 9 23.213 −32.843 −16.047 1.00 24.63 H C ATOM 3586 C6 THY H 9 24.278 −30.911 −17.223 1.00 25.76 H C ATOM 3587 P ADE H 10 27.345 −25.528 −17.528 1.00 25.05 H P ATOM 3588 OP1 ADE H 10 28.142 −24.542 −18.294 1.00 24.87 H O ATOM 3589 OP2 ADE H 10 27.446 −25.572 −16.053 1.00 32.93 H O ATOM 3590 O5′ ADE H 10 25.801 −25.365 −17.942 1.00 36.94 H O ATOM 3591 C5′ ADE H 10 25.438 −25.334 −19.320 1.00 27.06 H C ATOM 3592 C4′ ADE H 10 24.104 −24.641 −19.578 1.00 21.71 H C ATOM 3593 O4′ ADE H 10 22.992 −25.552 −19.403 1.00 23.14 H O ATOM 3594 C3′ ADE H 10 23.766 −23.430 −18.718 1.00 26.15 H C ATOM 3595 O3′ ADE H 10 23.199 −22.479 −19.609 1.00 22.80 H O ATOM 3596 C2′ ADE H 10 22.770 −23.973 −17.689 1.00 21.76 H C ATOM 3597 C1′ ADE H 10 22.042 −25.053 −18.482 1.00 22.72 H C ATOM 3598 N9 ADE H 10 21.627 −26.239 −17.736 1.00 25.17 H N ATOM 3599 C8 ADE H 10 22.386 −26.936 −16.836 1.00 21.36 H C ATOM 3600 N7 ADE H 10 21.773 −27.981 −16.336 1.00 23.59 H N ATOM 3601 C5 ADE H 10 20.529 −27.975 −16.953 1.00 20.38 H C ATOM 3602 C6 ADE H 10 19.407 −28.827 −16.848 1.00 23.03 H C ATOM 3603 N6 ADE H 10 19.372 −29.896 −16.046 1.00 23.54 H N ATOM 3604 N1 ADE H 10 18.319 −28.541 −17.599 1.00 21.58 H N ATOM 3605 C2 ADE H 10 18.362 −27.467 −18.396 1.00 22.37 H C ATOM 3606 N3 ADE H 10 19.360 −26.599 −18.579 1.00 22.34 H N ATOM 3607 C4 ADE H 10 20.426 −26.909 −17.824 1.00 19.27 H C ATOM 3608 P ADE H 11 22.583 −21.095 −19.118 1.00 26.29 H P ATOM 3609 OP1 ADE H 11 22.825 −20.107 −20.187 1.00 33.92 H O ATOM 3610 OP2 ADE H 11 23.049 −20.823 −17.739 1.00 23.74 H O ATOM 3611 O5′ ADE H 11 21.019 −21.433 −19.082 1.00 30.07 H O ATOM 3612 C5′ ADE H 11 20.386 −21.868 −20.271 1.00 23.89 H C ATOM 3613 C4′ ADE H 11 18.893 −22.085 −20.087 1.00 26.01 H C ATOM 3614 O4′ ADE H 11 18.646 −23.201 −19.196 1.00 21.90 H O ATOM 3615 C3′ ADE H 11 18.092 −20.920 −19.519 1.00 27.43 H C ATOM 3616 O3′ ADE H 11 16.835 −20.955 −20.172 1.00 27.25 H O ATOM 3617 C2′ ADE H 11 17.979 −21.286 −18.042 1.00 22.72 H C ATOM 3618 C1′ ADE H 11 17.810 −22.801 −18.134 1.00 25.26 H C ATOM 3619 N9 ADE H 11 18.307 −23.581 −17.012 1.00 25.82 H N ATOM 3620 C8 ADE H 11 19.473 −23.388 −16.320 1.00 25.44 H C ATOM 3621 N7 ADE H 11 19.678 −24.271 −15.368 1.00 26.30 H N ATOM 3622 C5 ADE H 11 18.573 −25.103 −15.458 1.00 24.43 H C ATOM 3623 C6 ADE H 11 18.193 −26.240 −14.727 1.00 27.00 H C ATOM 3624 N6 ADE H 11 18.934 −26.728 −13.724 1.00 30.82 H N ATOM 3625 N1 ADE H 11 17.027 −26.842 −15.058 1.00 26.79 H N ATOM 3626 C2 ADE H 11 16.298 −26.332 −16.063 1.00 27.42 H C ATOM 3627 N3 ADE H 11 16.557 −25.265 −16.826 1.00 24.29 H N ATOM 3628 C4 ADE H 11 17.720 −24.697 −16.468 1.00 22.11 H C ATOM 3629 P THY H 12 15.843 −19.698 −20.193 1.00 25.52 H P ATOM 3630 OP1 THY H 12 15.307 −19.601 −21.571 1.00 25.80 H O ATOM 3631 OP2 THY H 12 16.525 −18.534 −19.586 1.00 21.54 H O ATOM 3632 O5′ THY H 12 14.679 −20.166 −19.189 1.00 24.83 H O ATOM 3633 C5′ THY H 12 13.875 −21.310 −19.552 1.00 23.42 H C ATOM 3634 C4′ THY H 12 13.066 −21.839 −18.381 1.00 25.89 H C ATOM 3635 O4′ THY H 12 13.908 −22.629 −17.499 1.00 23.76 H O ATOM 3636 C3′ THY H 12 12.424 −20.761 −17.504 1.00 26.04 H C ATOM 3637 O3′ THY H 12 11.060 −21.064 −17.263 1.00 25.66 H O ATOM 3638 C2′ THY H 12 13.230 −20.844 −16.208 1.00 20.86 H C ATOM 3639 C1′ THY H 12 13.490 −22.343 −16.179 1.00 22.54 H C ATOM 3640 N1 THY H 12 14.533 −22.765 −15.212 1.00 22.51 H N ATOM 3641 C2 THY H 12 14.403 −23.972 −14.554 1.00 23.00 H C ATOM 3642 O2 THY H 12 13.472 −24.737 −14.721 1.00 21.72 H O ATOM 3643 N3 THY H 12 15.419 −24.266 −13.684 1.00 20.48 H N ATOM 3644 C4 THY H 12 16.523 −23.486 −13.419 1.00 20.15 H C ATOM 3645 O4 THY H 12 17.373 −23.849 −12.617 1.00 25.63 H O ATOM 3646 C5 THY H 12 16.597 −22.234 −14.136 1.00 18.49 H C ATOM 3647 C7 THY H 12 17.746 −21.289 −13.933 1.00 19.45 H C ATOM 3648 C6 THY H 12 15.613 −21.936 −14.987 1.00 18.74 H C ATOM 3649 P ADE H 13 9.921 −20.818 −18.362 1.00 34.68 H P ATOM 3650 OP1 ADE H 13 10.331 −21.523 −19.601 1.00 29.00 H O ATOM 3651 OP2 ADE H 13 9.602 −19.371 −18.385 1.00 23.43 H O ATOM 3652 O5′ ADE H 13 8.680 −21.612 −17.735 1.00 31.48 H O ATOM 3653 C5′ ADE H 13 8.703 −23.042 −17.751 1.00 29.17 H C ATOM 3654 C4′ ADE H 13 7.813 −23.633 −16.668 1.00 34.37 H C ATOM 3655 O4′ ADE H 13 8.562 −23.903 −15.452 1.00 29.36 H O ATOM 3656 C3′ ADE H 13 6.624 −22.779 −16.250 1.00 24.78 H C ATOM 3657 O3′ ADE H 13 5.562 −23.684 −15.966 1.00 27.24 H O ATOM 3658 C2′ ADE H 13 7.157 −22.038 −15.022 1.00 23.76 H C ATOM 3659 C1′ ADE H 13 8.208 −22.983 −14.437 1.00 26.59 H C ATOM 3660 N9 ADE H 13 9.444 −22.331 −14.012 1.00 23.20 H N ATOM 3661 C8 ADE H 13 9.886 −21.086 −14.361 1.00 19.68 H C ATOM 3662 N7 ADE H 13 11.043 −20.769 −13.826 1.00 21.48 H N ATOM 3663 C5 ADE H 13 11.394 −21.887 −13.084 1.00 20.04 H C ATOM 3664 C6 ADE H 13 12.518 −22.191 −12.283 1.00 20.93 H C ATOM 3665 N6 ADE H 13 13.542 −21.349 −12.085 1.00 17.98 H N ATOM 3666 N1 ADE H 13 12.548 −23.401 −11.684 1.00 21.14 H N ATOM 3667 C2 ADE H 13 11.525 −24.241 −11.878 1.00 21.71 H C ATOM 3668 N3 ADE H 13 10.422 −24.069 −12.608 1.00 21.94 H N ATOM 3669 C4 ADE H 13 10.417 −22.860 −13.191 1.00 21.50 H C ATOM 3670 P GUA H 14 4.132 −23.212 −15.419 1.00 31.73 H P ATOM 3671 OP1 GUA H 14 3.121 −24.184 −15.895 1.00 30.37 H O ATOM 3672 OP2 GUA H 14 3.978 −21.769 −15.712 1.00 29.29 H O ATOM 3673 O5′ GUA H 14 4.287 −23.434 −13.842 1.00 22.88 H O ATOM 3674 C5′ GUA H 14 4.449 −24.775 −13.402 1.00 30.01 H C ATOM 3675 C4′ GUA H 14 4.825 −24.840 −11.937 1.00 36.42 H C ATOM 3676 O4′ GUA H 14 6.132 −24.244 −11.745 1.00 33.71 H O ATOM 3677 C3′ GUA H 14 3.857 −24.124 −11.000 1.00 42.57 H C ATOM 3678 O3′ GUA H 14 3.409 −25.076 −10.033 1.00 51.87 H O ATOM 3679 C2′ GUA H 14 4.680 −22.978 −10.410 1.00 36.34 H C ATOM 3680 C1′ GUA H 14 6.119 −23.462 −10.575 1.00 30.10 H C ATOM 3681 N9 GUA H 14 7.096 −22.389 −10.734 1.00 29.80 H N ATOM 3682 C8 GUA H 14 6.985 −21.257 −11.508 1.00 28.65 H C ATOM 3683 N7 GUA H 14 8.033 −20.476 −11.442 1.00 26.36 H N ATOM 3684 C5 GUA H 14 8.890 −21.137 −10.574 1.00 23.38 H C ATOM 3685 C6 GUA H 14 10.174 −20.779 −10.118 1.00 25.14 H C ATOM 3686 O6 GUA H 14 10.832 −19.768 −10.404 1.00 27.81 H O ATOM 3687 N1 GUA H 14 10.694 −21.728 −9.239 1.00 24.30 H N ATOM 3688 C2 GUA H 14 10.052 −22.880 −8.854 1.00 28.25 H C ATOM 3689 N2 GUA H 14 10.706 −23.682 −8.003 1.00 28.77 H N ATOM 3690 N3 GUA H 14 8.849 −23.227 −9.279 1.00 31.04 H N ATOM 3691 C4 GUA H 14 8.330 −22.312 −10.131 1.00 29.88 H C ATOM 3692 P CYT H 15 2.723 −24.657 −8.650 1.00 56.18 H P ATOM 3693 OP1 CYT H 15 1.801 −25.752 −8.276 1.00 65.42 H O ATOM 3694 OP2 CYT H 15 2.225 −23.265 −8.747 1.00 43.75 H O ATOM 3695 O5′ CYT H 15 3.957 −24.676 −7.638 1.00 59.78 H O ATOM 3696 C5′ CYT H 15 4.712 −25.868 −7.488 1.00 59.36 H C ATOM 3697 C4′ CYT H 15 5.779 −25.661 −6.431 1.00 62.35 H C ATOM 3698 O4′ CYT H 15 6.708 −24.634 −6.865 1.00 55.00 H O ATOM 3699 C3′ CYT H 15 5.233 −25.203 −5.085 1.00 62.43 H C ATOM 3700 O3′ CYT H 15 5.961 −25.845 −4.045 1.00 67.79 H O ATOM 3701 C2′ CYT H 15 5.457 −23.692 −5.113 1.00 53.40 H C ATOM 3702 C1′ CYT H 15 6.753 −23.591 −5.910 1.00 48.72 H C ATOM 3703 N1 CYT H 15 6.917 −22.294 −6.633 1.00 40.77 H N ATOM 3704 C2 CYT H 15 8.077 −21.547 −6.422 1.00 37.46 H C ATOM 3705 O2 CYT H 15 8.931 −21.987 −5.643 1.00 37.14 H O ATOM 3706 N3 CYT H 15 8.232 −20.370 −7.075 1.00 31.15 H N ATOM 3707 C4 CYT H 15 7.280 −19.941 −7.906 1.00 35.33 H C ATOM 3708 N4 CYT H 15 7.478 −18.772 −8.528 1.00 30.93 H N ATOM 3709 C5 CYT H 15 6.084 −20.690 −8.137 1.00 34.65 H C ATOM 3710 C6 CYT H 15 5.946 −21.850 −7.485 1.00 36.08 H C ATOM 3711 P THY H 16 5.394 −25.882 −2.548 1.00 79.66 H P ATOM 3712 OP1 THY H 16 5.429 −27.295 −2.109 1.00 68.24 H O ATOM 3713 OP2 THY H 16 4.135 −25.097 −2.487 1.00 58.67 H O ATOM 3714 O5′ THY H 16 6.493 −25.054 −1.734 1.00 73.70 H O ATOM 3715 C5′ THY H 16 7.875 −25.332 −1.897 1.00 64.00 H C ATOM 3716 C4′ THY H 16 8.688 −24.210 −1.280 1.00 60.98 H C ATOM 3717 O4′ THY H 16 8.737 −23.062 −2.166 1.00 55.58 H O ATOM 3718 C3′ THY H 16 8.136 −23.697 0.047 1.00 64.34 H C ATOM 3719 O3′ THY H 16 9.212 −23.604 0.971 1.00 64.61 H O ATOM 3720 C2′ THY H 16 7.538 −22.334 −0.308 1.00 58.02 H C ATOM 3721 C1′ THY H 16 8.491 −21.892 −1.412 1.00 48.05 H C ATOM 3722 N1 THY H 16 7.964 −20.856 −2.347 1.00 44.06 H N ATOM 3723 C2 THY H 16 8.769 −19.783 −2.664 1.00 41.43 H C ATOM 3724 O2 THY H 16 9.893 −19.629 −2.209 1.00 36.22 H O ATOM 3725 N3 THY H 16 8.205 −18.887 −3.539 1.00 36.83 H N ATOM 3726 C4 THY H 16 6.950 −18.959 −4.114 1.00 37.73 H C ATOM 3727 O4 THY H 16 6.531 −18.106 −4.890 1.00 38.17 H O ATOM 3728 C5 THY H 16 6.164 −20.105 −3.738 1.00 39.00 H C ATOM 3729 C7 THY H 16 4.787 −20.274 −4.306 1.00 36.71 H C ATOM 3730 C6 THY H 16 6.700 −20.990 −2.886 1.00 42.86 H C ATOM 3731 P THY H 17 8.919 −23.580 2.540 1.00 80.14 H P ATOM 3732 OP1 THY H 17 9.864 −24.510 3.199 1.00 54.65 H O ATOM 3733 OP2 THY H 17 7.458 −23.738 2.723 1.00 73.46 H O ATOM 3734 O5′ THY H 17 9.297 −22.079 2.943 1.00 75.28 H O ATOM 3735 C5′ THY H 17 10.651 −21.640 2.934 1.00 69.65 H C ATOM 3736 C4′ THY H 17 10.703 −20.132 3.111 1.00 70.06 H C ATOM 3737 O4′ THY H 17 10.081 −19.502 1.961 1.00 61.48 H O ATOM 3738 C3′ THY H 17 9.974 −19.599 4.346 1.00 63.21 H C ATOM 3739 O3′ THY H 17 10.758 −18.600 4.997 1.00 62.30 H O ATOM 3740 C2′ THY H 17 8.674 −19.028 3.783 1.00 62.44 H C ATOM 3741 C1′ THY H 17 9.119 −18.566 2.400 1.00 65.67 H C ATOM 3742 N1 THY H 17 8.020 −18.547 1.409 1.00 62.67 H N ATOM 3743 C2 THY H 17 8.090 −17.678 0.342 1.00 57.28 H C ATOM 3744 O2 THY H 17 9.023 −16.913 0.165 1.00 46.63 H O ATOM 3745 N3 THY H 17 7.019 −17.741 −0.515 1.00 45.14 H N ATOM 3746 C4 THY H 17 5.915 −18.568 −0.407 1.00 46.53 H C ATOM 3747 O4 THY H 17 5.002 −18.549 −1.227 1.00 52.84 H O ATOM 3748 C5 THY H 17 5.910 −19.451 0.738 1.00 55.61 H C ATOM 3749 C7 THY H 17 4.766 −20.397 0.969 1.00 59.50 H C ATOM 3750 C6 THY H 17 6.950 −19.398 1.581 1.00 61.26 H C ATOM 1 C1 BML 100 1.351 −22.636 17.329 1.00 20.00 C ATOM 2 N1 BML 100 −2.345 −22.477 17.385 1.00 20.00 N ATOM 3 O1 BML 100 −2.760 −23.946 19.172 1.00 20.00 O ATOM 4 C10 BML 100 −4.869 −20.497 19.319 1.00 20.00 C ATOM 5 C11 BML 100 −5.507 −19.741 20.482 1.00 20.00 C ATOM 6 C12 BML 100 −5.137 −18.259 20.457 1.00 20.00 C ATOM 7 C13 BML 100 −5.895 −17.473 21.526 1.00 20.00 C ATOM 8 C14 BML 100 −5.909 −15.978 21.264 1.00 20.00 C ATOM 9 C15 BML 100 −7.826 −14.603 22.201 1.00 20.00 C ATOM 10 C16 BML 100 −7.966 −13.378 21.524 1.00 20.00 C ATOM 11 C17 BML 100 −9.198 −12.742 21.447 1.00 20.00 C ATOM 12 C18 BML 100 −10.316 −13.314 22.038 1.00 20.00 C ATOM 13 C19 BML 100 −10.196 −14.520 22.715 1.00 20.00 C ATOM 14 C2 BML 100 1.603 −23.425 16.212 1.00 20.00 C ATOM 15 O2 BML 100 −5.383 −15.494 20.271 1.00 20.00 O ATOM 16 N2 BML 100 −6.582 −15.302 22.279 1.00 20.00 N ATOM 17 C20 BML 100 −8.959 −15.167 22.831 1.00 20.00 C ATOM 18 C3 BML 100 0.544 −23.917 15.459 1.00 20.00 C ATOM 19 N3 BML 100 −8.917 −16.414 23.490 1.00 20.00 N ATOM 20 C4 BML 100 −0.770 −23.623 15.816 1.00 20.00 C ATOM 21 C5 BML 100 −1.039 −22.828 16.942 1.00 20.00 C ATOM 22 C6 BML 100 0.039 −22.340 17.692 1.00 20.00 C ATOM 23 C7 BML 100 −3.131 −23.145 18.322 1.00 20.00 C ATOM 24 C8 BML 100 −4.596 −22.775 18.212 1.00 20.00 C ATOM 25 C9 BML 100 −5.105 −22.006 19.432 1.00 20.00 C ATOM 1 C1 BML 200 22.035 3.898 −37.176 1.00 20.00 C ATOM 2 N1 BML 200 19.679 2.774 −39.797 1.00 20.00 N ATOM 3 O1 BML 200 17.888 2.589 −38.298 1.00 20.00 O ATOM 4 C10 BML 200 16.884 0.264 −42.287 1.00 20.00 C ATOM 5 C11 BML 200 16.812 −1.252 −42.480 1.00 20.00 C ATOM 6 C12 BML 200 15.887 −1.617 −43.642 1.00 20.00 C ATOM 7 C13 BML 200 15.592 −3.118 −43.719 1.00 20.00 C ATOM 8 C14 BML 200 14.527 −3.479 −44.739 1.00 20.00 C ATOM 9 C15 BML 200 13.205 −5.621 −44.418 1.00 20.00 C ATOM 10 C16 BML 200 12.291 −6.196 −45.320 1.00 20.00 C ATOM 11 C17 BML 200 11.237 −6.979 −44.865 1.00 20.00 C ATOM 12 C18 BML 200 11.075 −7.203 −43.507 1.00 20.00 C ATOM 13 C19 BML 200 11.958 −6.631 −42.603 1.00 20.00 C ATOM 14 C2 BML 200 23.026 2.924 −37.221 1.00 20.00 C ATOM 15 O2 BML 200 13.953 −2.593 −45.361 1.00 20.00 O ATOM 16 N2 BML 200 14.331 −4.854 −44.847 1.00 20.00 N ATOM 17 C20 BML 200 13.008 −5.810 −43.032 1.00 20.00 C ATOM 18 C3 BML 200 22.921 1.873 −38.124 1.00 20.00 C ATOM 19 N3 BML 200 13.896 −5.297 −42.064 1.00 20.00 N ATOM 20 C4 BML 200 21.833 1.792 −38.990 1.00 20.00 C ATOM 21 C5 BML 200 20.828 2.772 −38.956 1.00 20.00 C ATOM 22 C6 BML 200 20.940 3.819 −38.033 1.00 20.00 C ATOM 23 C7 BML 200 18.359 2.534 −39.426 1.00 20.00 C ATOM 24 C8 BML 200 17.500 2.146 −40.618 1.00 20.00 C ATOM 25 C9 BML 200 17.731 0.706 −41.088 1.00 20.00 C END

REFERENCES

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1. A method of modulating cellular processes, comprising: selecting a target transcription factor or co-factor related to a cellular process to be modulated; contacting said transcription factor or co-factor with an interfacial inhibitor, wherein said interfacial inhibitor is capable of selectively binding to a binding site located on an interface between said transcription factor or co-factor and a binding partner, thereby, disrupting the interactions between said transcription factor or co-factor with said binding partner.
 2. The method of claim 1, wherein said transcription co-factor is a HDAC enzyme.
 3. The method of claim 2, wherein said HDAC enzyme is one selected from the group consisting of class I and II HDACs.
 4. The method of claim 2, wherein said HDAC enzyme is one selected from the group consisting of class IIa HDACs.
 5. The method of claim 2, wherein said interfacial binding site is defined by the interface between said HDAC enzyme and MEF2.
 6. The method of claim 2, wherein said interfacial binding site is defined by the interface between said HDAC enzyme and a co-factor that recruit said HDAC to a target chromatin region.
 7. The method of claim 1, wherein said transcription factor is selected from the group consisting of MEF2, FOXP3.
 8. The method of claim 1, wherein said cellular process is one related to transcription dysregulation.
 9. The method of claim 1, wherein said interfacial inhibitor is a compound having a general formula of R^(a)-L-R^(b) capable of binding to a MEF2 interfacial binding site, and wherein: R^(a) is a recognition group that binds to the hydrophobic region of the MEF2 binding site selected from a group that includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—, R^(c)R^(d)N(SO₂)—, wherein: R^(c) and R^(d) are independently selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, alkylamino, dialkylamino, arylamino or heteroarylamino. L is a linker consisting of a chain of up to 20 carbon atoms, provided that up to three carbon atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that it can include substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro R^(b) is a recognition group that binds to the hydrophilic region of the MEF2 binding site selected from a group that includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—, R^(c)R^(d)N(SO₂)—, wherein: R^(c) and R^(d) are independently selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, alkylamino, dialkylamino, arylamino or heteroarylamino.
 10. The method of claim 1, wherein said interfacial inhibitor is a compound having a general formula of Ar¹-L¹-L²-L³-Ar² capable of binding to a MEF2 interfacial binding site, and wherein: Ar¹ and Ar² are aromatic rings independently selected from a group consisting of benzene, naphthalene, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, thiazole, isoxazole, indole, benzimidazole, benzothiazole, benzoxazole, provided that the aromatic ring may contain up to seven substituents selected from a group consisting of: hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, amino, alkylamino, dialkylamino, arylamino, heteroarylamino, hydroxy, or halo. The substituents can also join together to form a ring of up to 12 atoms, L¹ and L³ are linking groups independently selected from a group consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O), NR(C═O), S(═O) or —S(═O)₂— L² is a linking group selected from a group consisting of a chain of up to 10 carbon atoms, provided that up to three atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that these atoms can contain substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro
 11. The method of claim 1, wherein said interfacial inhibitor is a compound having a general formula of

wherein: R¹-R¹⁰ are independently selected from a group consisting of L¹ and L³ are linking groups independently selected from a group consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O), NR(C═O), S(═O) or —S(═O)₂— L² is a linking group selected from a group consisting of a chain of up to 10 carbon atoms, provided that up to three atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that these atoms can contain substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro.
 12. The method of claim 1, wherein said interfacial inhibitor is a compound capable of binding to a MEF2 interfacial binding site having a formula selected from a group consisting of:


13. A method of treating a patient suffering from a disease related to a transcription factor-dependent dysregulation, comprising: administering a pharmacologically effective amount of an interfacial inhibitor to the patient, wherein said interfacial inhibitor is one that is capable of binding selectively to a target transcription factor or its co-factor, wherein said transcription factor or co-factor is known to be related to the disease process.
 14. The method of claim 10, wherein said disease is one selected from transplant rejection, inflammation, autoimmune diseases, neurodegenerative diseases, cancer, and cardiovascular disease.
 15. The method of claim 10, wherein said transcription factor is one that recruits HDACs to a target DNA region.
 16. The method of claim 12, wherein said transcription factor is selected from MEF2, FOXP3, or combinations thereof.
 17. The method of claim 12, wherein said transcription co-factor is a member of HDACs.
 18. The method of claim 12, wherein said transcription co-factor is one selected from the group consisting of class I and II HDACs.
 19. The method of claim 12, wherein said HDAC deregulation related disease is one selected from the group consisting of cancer, neurodegenerative disease, heart disease, or combinations thereof.
 20. A method of identifying and optimizing an interfacial inhibitor for modulating interactions between a selected transcription factor or co-factor with its binding partner, comprising: a. obtaining a set of relative coordinates representing a crystal structure of said transcription factor or co-factor, or portions thereof containing functionally important interfaces, wherein said coordinates represent a conformation assumed by said transcription factor or co-factor when it is in a complexed state with its binding partner or a lead compound; and b. designing an inhibitor based on portions of said coordinates representing said interfaces.
 21. The method of claim 17, wherein said transcription factor is MEF2 or FOXP3.
 22. The method of claim 17, wherein said transcription co-factor is selected from the group consisting of class I and II HDAC.
 23. The method of claim 17, wherein said coordinates comprises beta strands S1, S2 and S3 and helix H2 of each MEF2 monomer in Table
 1. 24. The method of claim 17, wherein said coordinates are the coordinates in Table
 1. 25. An assay for screening, identifying, or optimizing a lead compound suitable for use as an interfacial inhibitor, comprising: providing an evaluating element, wherein said evaluating element comprises a molecular framework having a structure representing an interfacial binding site of a transcription factor or co-factor; contacting a test compound with said evaluating element; and identifying said test compound as a lead according to a predetermined response from the evaluating element.
 26. The assay of claim 25, wherein said evaluating element is a two-hybrid assay system having a binding domain fused to a selected transcription factor or co-factor, an activating domain fused to a binding partner of said transcription factor or co-factor, and a reporter gene, and wherein when said reporter signal falls below a predetermined level, the test compound is identified as a lead compound.
 27. The assay of claim 26, wherein said transcription factor is a member of MEF2D and said binding partner is a member of HDACs.
 28. The assay of claim 26, wherein said transcription factor is MEF2D and said binding partner is HDAC4 or an interacting portion thereof, wherein said interacting portion comprises the segment of HDAC4 that binds to MEF2D.
 29. The assay system of claim 25, wherein said transcription factor is one selected from MEF2, FOXP3, and other similar transcription factors that recruit HDACs to DNA.
 30. A kit for performing the assay of claim 26, comprising: a vector encoding said fused binding domain and acting domain.
 31. A compound useful for inhibiting binding between a selected HDAC and a transcription factor, said compound having a structural formula selected from any structure selected from a group consisting of:


32. The compound of claim 31, wherein said compound is useful as a NEF2 interfacial inhibitor.
 33. A compound useful as a MEF2 interfacial inhibitor, having a general formula of R^(a)-L-R^(b) capable of binding to a MEF2 interfacial binding site, wherein: R^(a) is a recognition group that binds to the hydrophobic region of the MEF2 binding site selected from a group that includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—, R^(c)R^(d)N(SO₂)—, wherein: R^(c) and R^(d) are independently selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, alkylamino, dialkylamino, arylamino or heteroarylamino. L is a linker consisting of a chain of up to 20 carbon atoms, provided that up to three carbon atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that it can include substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro R^(b) is a recognition group that binds to the hydrophilic region of the MEF2 binding site selected from a group that includes lower alkyl, alkenyl, alkynyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, or R^(c)R^(d)NC(═O)—, R^(c)R^(d)N(SO₂)—, wherein: R^(c) and R^(d) are independently selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, alkylamino, dialkylamino, arylamino or heteroarylamino.
 34. A compound useful as a MEF2 interfacial inhibitor, having a general formula of Ar¹-L¹-L²-L³-Ar² capable of binding to a MEF2 interfacial binding site, wherein: Ar¹ and Ar² are aromatic rings independently selected from a group consisting of benzene, naphthalene, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, pyrrole, furan, thiophene, imidazole, pyrazole, oxazole, thiazole, isoxazole, indole, benzimidazole, benzothiazole, benzoxazole, provided that the aromatic ring may contain up to seven substituents selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, amino, alkylamino, dialkylamino, arylamino, heteroarylamino, hydroxy, or halo. The substituents can also join together to form a ring of up to 12 atoms, L¹ and L³ are linking groups independently selected from a group consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O), NR(C═O), S(═O) or —S(═O)₂— L² is a linking group selected from a group consisting of a chain of up to 10 carbon atoms, provided that up to three atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that these atoms can contain substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro.
 35. A compound useful as a MEF2 interfacial inhibitor, having a general formula of

wherein: R¹-R¹⁰ are independently selected from a group consisting of L¹ and L³ are linking groups independently selected from a group consisting of amino, alkylamino, arylamino, oxa, keto, NHC(═O), NR(C═O), S(═O) or —S(═O)₂— L² is a linking group selected from a group consisting of a chain of up to 10 carbon atoms, provided that up to three atoms can be replaced with an oxygen, nitrogen or sulfur atom, and further provided that these atoms can contain substituents selected from a group consisting of: alkyl, alkenyl, alkynyl, aryl, heteroaryl, benzo, hydroxy, alkoxy, aryloxy, oxa, keto, amido, sulfonamido, or fluoro.
 36. A composition useful for modulating interactions between HDACs and NEF2, comprising a compound according to claims 31, 33, 34, 35, or combinations thereof. 